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Placenta hypoplasia

DA: 34

Developmental anomaly information

Definition: Placenta with high vascular resistence and villous maturation arrest

Developmental anomaly parent: (empty)	Topology: (empty)
System: (empty)	Developmental anomaly category: Anomaly of underdevelopment or overdevelopment

Case records MDB6, MDB15, MDB19, MDB29, MDB37, MDB39, MDB40, MDB46, MDB47, MDB49, MDB119, MDB54, MDB56, MDB62, MDB64, MDB86, MDB91, MDB100, MDB101, MDB103, MDB110, MDB122, MDB127, MDB136, MDB139, MDB154, MDB157, MDB169, MDB183, MDB184, MDB192, MDB385, MDB196, MDB200, MDB201, MDB208, MDB209, MDB210, MDB215, MDB219, MDB223, MDB224, MDB231, MDB242, MDB249, MDB255, MDB254, MDB261, MDB263, MDB266, MDB272, MDB273, MDB274, MDB275, MDB278, MDB282, MDB286, MDB287, MDB289, MDB293, MDB294, MDB303, MDB305, MDB310, MDB315, MDB316, MDB317, MDB321, MDB332, MDB333, MDB339, MDB358, MDB359, MDB369, MDB379, MDB382, MDB386, MDB396, MDB403, MDB414, MDB417, MDB419, MDB425, MDB434, MDB452, MDB463, MDB471, MDB473, MDB477, MDB483, MDB491, MDB492, MDB495, MDB496, MDB497, MDB503, MDB504, MDB513, MDB520, MDB522, MDB523, MDB526, MDB530, MDB531, MDB537, MDB543, MDB22, MDB102, MDB140, MDB162, MDB199, MDB221, MDB213, MDB222, MDB258, MDB259, MDB329, MDB338, MDB326, MDB48, MDB250, MDB268, MDB291, MDB301, MDB322, MDB320, MDB387, MDB171

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Humpath: 13298

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

() in cases MDB, MDB, MDB, MDB, MDB

Associated genes in profile

Associated genes in malformative diseases

Associated chromosomal diseases

Associated signaling pathways

Associated developmental anomalies

Here is the list of developmental anomalies associated with this developmental anomaly, based on the cases' information :

Pulmonary hypoplasia 4.15% (47/1132 anomalies), in cases MDB29, MDB37, MDB56, MDB100, MDB103, MDB122, MDB127, MDB183, MDB192, MDB200, MDB201, MDB209, MDB210, MDB223, MDB254, MDB261, MDB266, MDB273, MDB274, MDB275, MDB294, MDB316, MDB333, MDB359, MDB379, MDB382, MDB417, MDB463, MDB471, MDB477, MDB483, MDB495, MDB496, MDB497, MDB503, MDB530, MDB531, MDB537, MDB22, MDB221, MDB259, MDB329, MDB326, MDB268, MDB291, MDB322, MDB171
Intrauterine growth retardation, symmetric 3.89% (44/1132 anomalies), in cases MDB15, MDB86, MDB101, MDB103, MDB136, MDB215, MDB219, MDB223, MDB249, MDB254, MDB263, MDB266, MDB274, MDB275, MDB278, MDB286, MDB305, MDB310, MDB321, MDB332, MDB339, MDB358, MDB359, MDB396, MDB403, MDB414, MDB452, MDB471, MDB473, MDB477, MDB483, MDB495, MDB513, MDB520, MDB522, MDB22, MDB140, MDB162, MDB199, MDB329, MDB338, MDB291, MDB322, MDB387
Facial dysmorphism 3.53% (40/1132 anomalies), in cases MDB29, MDB37, MDB40, MDB47, MDB54, MDB56, MDB100, MDB101, MDB136, MDB139, MDB154, MDB200, MDB215, MDB261, MDB263, MDB266, MDB278, MDB286, MDB315, MDB317, MDB321, MDB332, MDB339, MDB358, MDB359, MDB452, MDB463, MDB471, MDB473, MDB504, MDB520, MDB522, MDB531, MDB543, MDB258, MDB329, MDB338, MDB48, MDB320, MDB171
Low-set ears 3.53% (40/1132 anomalies), in cases MDB29, MDB47, MDB100, MDB101, MDB103, MDB136, MDB196, MDB201, MDB209, MDB215, MDB223, MDB242, MDB249, MDB261, MDB287, MDB310, MDB321, MDB332, MDB339, MDB359, MDB419, MDB471, MDB473, MDB483, MDB491, MDB503, MDB504, MDB520, MDB522, MDB543, MDB22, MDB140, MDB162, MDB258, MDB329, MDB326, MDB48, MDB268, MDB387, MDB171
Talipes equinovarus, bilateral 1.68% (19/1132 anomalies), in cases MDB29, MDB119, MDB103, MDB110, MDB209, MDB215, MDB219, MDB223, MDB254, MDB266, MDB274, MDB310, MDB317, MDB333, MDB396, MDB417, MDB140, MDB338, MDB322
Micrognathia 1.68% (19/1132 anomalies), in cases MDB101, MDB157, MDB196, MDB200, MDB209, MDB242, MDB263, MDB274, MDB286, MDB287, MDB305, MDB310, MDB315, MDB317, MDB473, MDB48, MDB291, MDB320, MDB171
Hypertelorism 1.59% (18/1132 anomalies), in cases MDB47, MDB100, MDB136, MDB139, MDB154, MDB192, MDB196, MDB215, MDB315, MDB321, MDB358, MDB473, MDB491, MDB520, MDB522, MDB338, MDB322, MDB320
Broad nasal bridge 1.15% (13/1132 anomalies), in cases MDB40, MDB47, MDB100, MDB196, MDB215, MDB321, MDB497, MDB504, MDB520, MDB326, MDB48, MDB322, MDB320
Adrenal hypoplasia, fetal 1.15% (13/1132 anomalies), in cases MDB49, MDB385, MDB196, MDB201, MDB286, MDB316, MDB358, MDB403, MDB452, MDB477, MDB520, MDB526, MDB221
Microcephaly 1.06% (12/1132 anomalies), in cases MDB15, MDB54, MDB263, MDB315, MDB473, MDB22, MDB258, MDB259, MDB329, MDB326, MDB291, MDB322
Neck edema 1.06% (12/1132 anomalies), in cases MDB29, MDB200, MDB263, MDB310, MDB321, MDB419, MDB434, MDB496, MDB520, MDB523, MDB543, MDB322
Retrognathia 1.06% (12/1132 anomalies), in cases MDB40, MDB100, MDB136, MDB255, MDB332, MDB339, MDB358, MDB359, MDB471, MDB503, MDB504, MDB543
Short neck 1.06% (12/1132 anomalies), in cases MDB40, MDB215, MDB403, MDB417, MDB496, MDB140, MDB329, MDB338, MDB268, MDB322, MDB320, MDB387
Microretrognathia 1.06% (12/1132 anomalies), in cases MDB103, MDB201, MDB208, MDB223, MDB333, MDB403, MDB520, MDB523, MDB531, MDB258, MDB326, MDB322
Single umblical artery (SUA)-Isolated 0.97% (11/1132 anomalies), in cases MDB56, MDB209, MDB215, MDB278, MDB333, MDB358, MDB359, MDB382, MDB492, MDB496, MDB322
Overlapping fingers 0.88% (10/1132 anomalies), in cases MDB15, MDB91, MDB100, MDB101, MDB157, MDB201, MDB224, MDB22, MDB221, MDB322
Corpus callosum agenesis 0.88% (10/1132 anomalies), in cases MDB37, MDB54, MDB139, MDB219, MDB263, MDB473, MDB497, MDB258, MDB329, MDB291
Clindodactyly of 5th finger, bilateral 0.88% (10/1132 anomalies), in cases MDB56, MDB62, MDB196, MDB200, MDB215, MDB219, MDB315, MDB140, MDB48, MDB387
Coarctation of aorta, 0.88% (10/1132 anomalies), in cases MDB101, MDB136, MDB157, MDB219, MDB286, MDB333, MDB369, MDB537, MDB102, MDB268
Low nasal bridge 0.88% (10/1132 anomalies), in cases MDB103, MDB208, MDB223, MDB287, MDB305, MDB403, MDB471, MDB338, MDB268, MDB387
Flattened nose 0.8% (9/1132 anomalies), in cases MDB100, MDB209, MDB223, MDB255, MDB263, MDB140, MDB258, MDB329, MDB320
Lobulated, fused and horseshoe kidney 0.8% (9/1132 anomalies), in cases MDB101, MDB157, MDB310, MDB332, MDB359, MDB417, MDB477, MDB48, MDB320
Clindodactyly of 5th finger, unilateral 0.8% (9/1132 anomalies), in cases MDB136, MDB139, MDB224, MDB287, MDB305, MDB522, MDB22, MDB221, MDB338
Narrow thorax 0.71% (8/1132 anomalies), in cases MDB196, MDB223, MDB286, MDB294, MDB358, MDB471, MDB526, MDB259
Triangular face 0.71% (8/1132 anomalies), in cases MDB201, MDB223, MDB317, MDB332, MDB359, MDB452, MDB522, MDB22
Meckel diverticulum 0.62% (7/1132 anomalies), in cases MDB37, MDB101, MDB110, MDB127, MDB136, MDB157, MDB326
Defective developement of left ventricle 0.62% (7/1132 anomalies), in cases MDB39, MDB46, MDB64, MDB136, MDB183, MDB201, MDB463
Intestinal malrotation 0.62% (7/1132 anomalies), in cases MDB100, MDB122, MDB136, MDB379, MDB477, MDB504, MDB301
Potter deformity sequence 0.62% (7/1132 anomalies), in cases MDB103, MDB110, MDB209, MDB219, MDB223, MDB255, MDB503
Aberrant right subclavian artery 0.62% (7/1132 anomalies), in cases MDB122, MDB209, MDB463, MDB526, MDB22, MDB102, MDB268
Single transverse palmar crease, unilateral 0.62% (7/1132 anomalies), in cases MDB136, MDB242, MDB272, MDB305, MDB321, MDB268, MDB387
Prominent and pointed nose 0.62% (7/1132 anomalies), in cases MDB201, MDB201, MDB242, MDB286, MDB317, MDB332, MDB531
Nonimmune hydrops fetalis (NIHF) 0.62% (7/1132 anomalies), in cases MDB333, MDB339, MDB483, MDB495, MDB537, MDB102, MDB162
Cerebral ventriculomegaly 0.53% (6/1132 anomalies), in cases MDB15, MDB303, MDB497, MDB520, MDB537, MDB199
Multicystic renal dysplasia,bilateral 0.53% (6/1132 anomalies), in cases MDB29, MDB215, MDB255, MDB278, MDB496, MDB320
Thalamic nuclei centrum medianum fusion 0.53% (6/1132 anomalies), in cases MDB37, MDB54, MDB263, MDB258, MDB329, MDB291
Exophthalmos, bilateral 0.53% (6/1132 anomalies), in cases MDB47, MDB263, MDB286, MDB358, MDB496, MDB140
Omphalocele 0.53% (6/1132 anomalies), in cases MDB119, MDB100, MDB184, MDB249, MDB359, MDB22
Microstomia 0.53% (6/1132 anomalies), in cases MDB54, MDB157, MDB305, MDB434, MDB291, MDB320
Ventricular septal defect, muscular 0.53% (6/1132 anomalies), in cases MDB101, MDB157, MDB452, MDB526, MDB22, MDB329
Sloping forehead 0.53% (6/1132 anomalies), in cases MDB154, MDB200, MDB201, MDB258, MDB326, MDB322
Camptodactyly, bilateral 0.53% (6/1132 anomalies), in cases MDB201, MDB266, MDB316, MDB396, MDB504, MDB322
Tetralogy of Fallot 0.53% (6/1132 anomalies), in cases MDB208, MDB491, MDB492, MDB504, MDB513, MDB326
Imperforate Anus 0.53% (6/1132 anomalies), in cases MDB208, MDB209, MDB255, MDB382, MDB492, MDB222
Bladder hypoplasia 0.53% (6/1132 anomalies), in cases MDB209, MDB278, MDB310, MDB503, MDB531, MDB213
Triploidy, Maternal, nonmolar (triploidy by digyny) 0.53% (6/1132 anomalies), in cases MDB286, MDB332, MDB358, MDB477, MDB543, MDB171
Renal agenesis, unilateral 0.44% (5/1132 anomalies), in cases MDB15, MDB19, MDB358, MDB382, MDB503
Cerebellar hypoplasia 0.44% (5/1132 anomalies), in cases MDB15, MDB310, MDB315, MDB329, MDB291
Absence of one paire the rib 0.44% (5/1132 anomalies), in cases MDB19, MDB56, MDB273, MDB483, MDB326
Long philtrum 0.44% (5/1132 anomalies), in cases MDB29, MDB531, MDB329, MDB322, MDB320
Cleft palate with cleft lip,bilateral, complete 0.44% (5/1132 anomalies), in cases MDB37, MDB261, MDB417, MDB326, MDB301
Aortic valve stenosis, congenital 0.44% (5/1132 anomalies), in cases MDB46, MDB127, MDB136, MDB183, MDB201
Hypoplasia of ascending aorta 0.44% (5/1132 anomalies), in cases MDB46, MDB64, MDB127, MDB201, MDB301
Macrocephaly 0.44% (5/1132 anomalies), in cases MDB47, MDB100, MDB208, MDB358, MDB379
Syndactyly of the feet , simple (webbed), unilateral 0.44% (5/1132 anomalies), in cases MDB49, MDB101, MDB196, MDB310, MDB322
Arthrogryposis 0.44% (5/1132 anomalies), in cases MDB110, MDB520, MDB522, MDB543, MDB329
Potter's facies 0.44% (5/1132 anomalies), in cases MDB110, MDB209, MDB219, MDB223, MDB255
Right atrium Enlargement 0.44% (5/1132 anomalies), in cases MDB136, MDB201, MDB208, MDB513, MDB326
Renal hypoplasia 0.44% (5/1132 anomalies), in cases MDB196, MDB287, MDB289, MDB379, MDB171
Pulmonary artery hypoplasia 0.44% (5/1132 anomalies), in cases MDB208, MDB293, MDB477, MDB504, MDB326
Toe hypoplasia, first, bilateral 0.44% (5/1132 anomalies), in cases MDB242, MDB254, MDB263, MDB310, MDB414
Polydactyly of the hand, preaxial 0.44% (5/1132 anomalies), in cases MDB249, MDB473, MDB513, MDB322, MDB322
Decreased skull bone mineralization 0.44% (5/1132 anomalies), in cases MDB254, MDB261, MDB266, MDB289, MDB294
Giant omphalocele 0.35% (4/1132 anomalies), in cases MDB29, MDB473, MDB491, MDB492
Foot edema 0.35% (4/1132 anomalies), in cases MDB29, MDB520, MDB523, MDB162
Hypotelorisme 0.35% (4/1132 anomalies), in cases MDB37, MDB463, MDB504, MDB326
Posteriorly inclined and low-positioned ears 0.35% (4/1132 anomalies), in cases MDB40, MDB425, MDB496, MDB320
Pulmonary artery dilatation, fetal 0.35% (4/1132 anomalies), in cases MDB46, MDB64, MDB136, MDB332
Persistent left superior vena cava 0.35% (4/1132 anomalies), in cases MDB122, MDB209, MDB414, MDB22
Retroplacental hemorrhage 0.35% (4/1132 anomalies), in cases MDB169, MDB184, MDB543, MDB326
Intrauterine growth retardation, asymmetric 0.35% (4/1132 anomalies), in cases MDB192, MDB196, MDB273, MDB282
Relative Macrocephaly 0.35% (4/1132 anomalies), in cases MDB196, MDB273, MDB414, MDB477
Wide space between 1st and 2nd toes, bilateral 0.35% (4/1132 anomalies), in cases MDB196, MDB266, MDB287, MDB305
Nasal hypoplasia 0.35% (4/1132 anomalies), in cases MDB200, MDB263, MDB417, MDB483
Cleft palate, median posterior 0.35% (4/1132 anomalies), in cases MDB215, MDB425, MDB513, MDB320
Single cerebral ventricule 0.35% (4/1132 anomalies), in cases MDB263, MDB473, MDB258, MDB291
Gothic palate 0.35% (4/1132 anomalies), in cases MDB263, MDB496, MDB322, MDB320
Bowing of long bones 0.35% (4/1132 anomalies), in cases MDB266, MDB274, MDB289, MDB294
Brachydactyly 0.35% (4/1132 anomalies), in cases MDB274, MDB287, MDB305, MDB483
Limbs hypoplasia 0.35% (4/1132 anomalies), in cases MDB274, MDB278, MDB471, MDB483
Hypogenesis of the Cerebellar Vermis 0.35% (4/1132 anomalies), in cases MDB278, MDB310, MDB359, MDB329
Long umbilical cord 0.35% (4/1132 anomalies), in cases MDB278, MDB310, MDB522, MDB291
Ventricular septal defect, membranous 0.35% (4/1132 anomalies), in cases MDB310, MDB434, MDB326, MDB387
Syndactyly of the fingers, complex, bilateral 0.35% (4/1132 anomalies), in cases MDB332, MDB358, MDB477, MDB171
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.35% (4/1132 anomalies), in cases MDB379, MDB22, MDB22, MDB222
Dextroposition of aorta 0.35% (4/1132 anomalies), in cases MDB434, MDB504, MDB513, MDB326
Cystic hygroma 0.35% (4/1132 anomalies), in cases MDB495, MDB537, MDB259, MDB329
Cleft palate with cleft lip, unilateral, complete 0.27% (3/1132 anomalies), in cases MDB15, MDB86, MDB221
Cubital deviation of the hand, unilateral 0.27% (3/1132 anomalies), in cases MDB19, MDB224, MDB537
Epicanthus 0.27% (3/1132 anomalies), in cases MDB29, MDB139, MDB200
Myelomeningocele, lumbosacral 0.27% (3/1132 anomalies), in cases MDB37, MDB386, MDB396
Polydactyly of both fingers & toes, postaxial 0.27% (3/1132 anomalies), in cases MDB37, MDB136, MDB434
Micropenis 0.27% (3/1132 anomalies), in cases MDB37, MDB196, MDB326
Nephromegaly, bilateral 0.27% (3/1132 anomalies), in cases MDB37, MDB278, MDB213
Splenomegaly, congenital 0.27% (3/1132 anomalies), in cases MDB37, MDB333, MDB463
Right ventricle dilatation 0.27% (3/1132 anomalies), in cases MDB46, MDB136, MDB201
Hydrocephalus 0.27% (3/1132 anomalies), in cases MDB47, MDB100, MDB322
Syndactyly of the toes, unilateral 0.27% (3/1132 anomalies), in cases MDB49, MDB278, MDB171
Right bilobate lung 0.27% (3/1132 anomalies), in cases MDB49, MDB196, MDB215
Syndactyly, simple (webbed), fingers 0.27% (3/1132 anomalies), in cases MDB49, MDB224, MDB286
Absence of diaphragm, left 0.27% (3/1132 anomalies), in cases MDB119, MDB434, MDB483
Semilobar holoprosencephaly 0.27% (3/1132 anomalies), in cases MDB54, MDB473, MDB258
Olfactory bulbs, absence of 0.27% (3/1132 anomalies), in cases MDB54, MDB258, MDB291
Diaphragmatic hernia, congenital 0.27% (3/1132 anomalies), in cases MDB56, MDB100, MDB122
Aortic valve atresia 0.27% (3/1132 anomalies), in cases MDB64, MDB101, MDB332
Mitral valve stenosis 0.27% (3/1132 anomalies), in cases MDB64, MDB127, MDB183
Renal agenesis, bilateral 0.27% (3/1132 anomalies), in cases MDB110, MDB209, MDB531
Anencephaly 0.27% (3/1132 anomalies), in cases MDB122, MDB496, MDB140
Infarcted placenta 0.27% (3/1132 anomalies), in cases MDB192, MDB208, MDB369
Frontal bossing 0.27% (3/1132 anomalies), in cases MDB196, MDB223, MDB471
Short philtrum 0.27% (3/1132 anomalies), in cases MDB196, MDB473, MDB258
Macroglossia 0.27% (3/1132 anomalies), in cases MDB200, MDB496, MDB171
Mongoloid slope of the palpebral fissures 0.27% (3/1132 anomalies), in cases MDB200, MDB419, MDB338
Right ventricular hypertrophy 0.27% (3/1132 anomalies), in cases MDB208, MDB504, MDB513
Micromelia 0.27% (3/1132 anomalies), in cases MDB215, MDB266, MDB282
Short umbilical cord 0.27% (3/1132 anomalies), in cases MDB219, MDB483, MDB491
Cleft palate, bilateral 0.27% (3/1132 anomalies), in cases MDB249, MDB332, MDB452
Dilatation of ureter , bilateral, congenital 0.27% (3/1132 anomalies), in cases MDB255, MDB329, MDB320
Osteogenesis imperfecta, Type II 0.27% (3/1132 anomalies), in cases MDB254, MDB266, MDB289
Arhinia 0.27% (3/1132 anomalies), in cases MDB261, MDB434, MDB291
Holoprosencephaly, lobar 0.27% (3/1132 anomalies), in cases MDB263, MDB329, MDB291
Camptodactyly, unilateral 0.27% (3/1132 anomalies), in cases MDB275, MDB278, MDB496
Polymicrogyria, focal 0.27% (3/1132 anomalies), in cases MDB369, MDB329, MDB329
Megacystis 0.27% (3/1132 anomalies), in cases MDB382, MDB329, MDB320
Large anterior fontanelle 0.27% (3/1132 anomalies), in cases MDB414, MDB471, MDB543
Ambiguous genitalia 0.27% (3/1132 anomalies), in cases MDB414, MDB477, MDB531
Polydactyly,of the hand, postaxial 0.27% (3/1132 anomalies), in cases MDB463, MDB473, MDB301
Thymic hypoplasia 0.27% (3/1132 anomalies), in cases MDB483, MDB513, MDB326
Large nose, fetal 0.27% (3/1132 anomalies), in cases MDB531, MDB543, MDB171
Hydronephrosis, congenital, bilateral 0.27% (3/1132 anomalies), in cases MDB329, MDB250, MDB320
Encephalocele, occipital 0.18% (2/1132 anomalies), in cases MDB6, MDB497
Microtia 0.18% (2/1132 anomalies), in cases MDB15, MDB37
absence of radius, bilateral 0.18% (2/1132 anomalies), in cases MDB19, MDB40
Thumb agenesis, unilateral 0.18% (2/1132 anomalies), in cases MDB19, MDB140
Holoprosencephaly, alobar 0.18% (2/1132 anomalies), in cases MDB37, MDB463
Flattened occiput 0.18% (2/1132 anomalies), in cases MDB40, MDB417
Thin upper lip 0.18% (2/1132 anomalies), in cases MDB47, MDB320
Unilobate lung, unilateral 0.18% (2/1132 anomalies), in cases MDB49, MDB215
Scoliosis, congenital 0.18% (2/1132 anomalies), in cases MDB119, MDB86
Pulmonary lobation anomalies 0.18% (2/1132 anomalies), in cases MDB119, MDB477
Ectopia cordis 0.18% (2/1132 anomalies), in cases MDB119, MDB119
Anophthalmos, bilateral 0.18% (2/1132 anomalies), in cases MDB54, MDB291
Ductus arteriosus dilatation 0.18% (2/1132 anomalies), in cases MDB64, MDB369
Fingers amputation 0.18% (2/1132 anomalies), in cases MDB86, MDB224
Renal focal cystic dilatation of collecting tubules 0.18% (2/1132 anomalies), in cases MDB100, MDB275
Placenta circumvallata 0.18% (2/1132 anomalies), in cases MDB103, MDB379
Absence of innominate (brachiocephalic) vein 0.18% (2/1132 anomalies), in cases MDB122, MDB22
Flexion contracture of the fingers 0.18% (2/1132 anomalies), in cases MDB196, MDB322
Rocker-bottom feet 0.18% (2/1132 anomalies), in cases MDB196, MDB522
Small round skull 0.18% (2/1132 anomalies), in cases MDB201, MDB322
Transverse aortic hypoplasia 0.18% (2/1132 anomalies), in cases MDB201, MDB495
Patent Foramen Ovale 0.18% (2/1132 anomalies), in cases MDB201, MDB208
Pulmonary valve hypoplasia, congenital 0.18% (2/1132 anomalies), in cases MDB208, MDB513
Persistent truncus arteriosus 0.18% (2/1132 anomalies), in cases MDB208, MDB452
Ureter agenesis, bilateral 0.18% (2/1132 anomalies), in cases MDB209, MDB531
Microphthalmia 0.18% (2/1132 anomalies), in cases MDB215, MDB261
Talipes equinovarus,unilateral 0.18% (2/1132 anomalies), in cases MDB224, MDB316
Hand edema 0.18% (2/1132 anomalies), in cases MDB224, MDB162
Autosomal Recessive Polycystic Kidney Disease 0.18% (2/1132 anomalies), in cases MDB231, MDB213
Syndactyly of the fingers, complex, unilateral 0.18% (2/1132 anomalies), in cases MDB249, MDB286
Arthrogryposis,lower limbs 0.18% (2/1132 anomalies), in cases MDB249, MDB275
Megarectum 0.18% (2/1132 anomalies), in cases MDB255, MDB222
Scoliosis, dextroconvex, thoracic 0.18% (2/1132 anomalies), in cases MDB273, MDB322
Placental hypermaturity 0.18% (2/1132 anomalies), in cases MDB282, MDB332
Limbs hypoplasia, lower extremities 0.18% (2/1132 anomalies), in cases MDB289, MDB530
Bowing of long bones of leg, congenital 0.18% (2/1132 anomalies), in cases MDB289, MDB530
Myelomeningocele,lumbosacral with hydrocephalus 0.18% (2/1132 anomalies), in cases MDB303, MDB417
Macrostomia 0.18% (2/1132 anomalies), in cases MDB315, MDB543
Hexadactyly, postaxial 0.18% (2/1132 anomalies), in cases MDB321, MDB326
Renal pelvis dilatation, unilateral 0.18% (2/1132 anomalies), in cases MDB321, MDB369
Syndactyly of the toes, complex, bilateral 0.18% (2/1132 anomalies), in cases MDB332, MDB477
Unilobate lung, bilateral 0.18% (2/1132 anomalies), in cases MDB358, MDB259
overlapping skull bones 0.18% (2/1132 anomalies), in cases MDB382, MDB386
Wide space between 1st and 2nd toes, unilateral 0.18% (2/1132 anomalies), in cases MDB414, MDB322
Cyclopia 0.18% (2/1132 anomalies), in cases MDB434, MDB291
Proboscis 0.18% (2/1132 anomalies), in cases MDB434, MDB463
Interauricular communication 0.18% (2/1132 anomalies), in cases MDB473, MDB326
Renal ectopia,crossed 0.18% (2/1132 anomalies), in cases MDB492, MDB503
Anencephaly facies 0.18% (2/1132 anomalies), in cases MDB496, MDB140
Bicornuate uterus 0.18% (2/1132 anomalies), in cases MDB503, MDB301
Neuronal migration anomaly 0.18% (2/1132 anomalies), in cases MDB258, MDB322
Olfactory nerve, absence of, bilateral 0.18% (2/1132 anomalies), in cases MDB258, MDB291
Badly-hemmed ears 0.18% (2/1132 anomalies), in cases MDB326, MDB320
Polysplenia 0.18% (2/1132 anomalies), in cases MDB326, MDB322
Communicating hydrocephalus 0.09% (1/1132 anomalies), in case MDB6
Myelomeningocele, thoracic 0.09% (1/1132 anomalies), in case MDB19
Relative Microcephaly 0.09% (1/1132 anomalies), in case MDB19
Axillary pterygia,unilateral 0.09% (1/1132 anomalies), in case MDB29
Tridactyly, unilateral 0.09% (1/1132 anomalies), in case MDB29
vertebral bones and gracile ribs with multiple abnormalities 0.09% (1/1132 anomalies), in case MDB29
Flat face 0.09% (1/1132 anomalies), in case MDB37
Rachischisis 0.09% (1/1132 anomalies), in case MDB37
Mitral valve atresia 0.09% (1/1132 anomalies), in case MDB39
Oligodactyly 0.09% (1/1132 anomalies), in case MDB40
Ulna,absence of, bilateral 0.09% (1/1132 anomalies), in case MDB40
Cornélia de Lange syndrome 0.09% (1/1132 anomalies), in case MDB40
short nose 0.09% (1/1132 anomalies), in case MDB40
Tetra-amelia 0.09% (1/1132 anomalies), in case MDB47
Lumbosacral agenesis 0.09% (1/1132 anomalies), in case MDB47
Parietal pericardium, absence of 0.09% (1/1132 anomalies), in case MDB119
Defects of the lower part of the sternum 0.09% (1/1132 anomalies), in case MDB119
Optic nerve, absence of, bilateral 0.09% (1/1132 anomalies), in case MDB54
Microglossia 0.09% (1/1132 anomalies), in case MDB54
cutaneous edema, fetal 0.09% (1/1132 anomalies), in case MDB56
Hypoplastic left heart syndrome (HLHS) 0.09% (1/1132 anomalies), in case MDB64
Encephalocele 0.09% (1/1132 anomalies), in case MDB86
Gastroschisis 0.09% (1/1132 anomalies), in case MDB86
Shortening (micromelia) of upper limb(s), unilateral 0.09% (1/1132 anomalies), in case MDB86
Pulmonary Cysts, congenital 0.09% (1/1132 anomalies), in case MDB86
Trilobate lung, bilateral 0.09% (1/1132 anomalies), in case MDB91
Syndactyly of the feet , simple (webbed), bilateral 0.09% (1/1132 anomalies), in case MDB101
Turned-up nose 0.09% (1/1132 anomalies), in case MDB101
Bone mineralization defect 0.09% (1/1132 anomalies), in case MDB103
Endocardial fibroelastosis 0.09% (1/1132 anomalies), in case MDB127
Hypoplasia of the aortic isthmus 0.09% (1/1132 anomalies), in case MDB127
Neuroepithelial cysts of the third ventricule,congenital 0.09% (1/1132 anomalies), in case MDB139
Cerebellar asymmetry 0.09% (1/1132 anomalies), in case MDB154
Brainstem asymmetry 0.09% (1/1132 anomalies), in case MDB154
Dentate nucleus malformation 0.09% (1/1132 anomalies), in case MDB154
Abnormal formation of the cerebellar gyri 0.09% (1/1132 anomalies), in case MDB154
Trilobate lung, left 0.09% (1/1132 anomalies), in case MDB183
Femural hypoplasia, unilateral 0.09% (1/1132 anomalies), in case MDB385
absence of peroneal bone, unilateral 0.09% (1/1132 anomalies), in case MDB385
Dislocation of the knee, congenital, unilateral 0.09% (1/1132 anomalies), in case MDB385
Arachnodactyly of the toes 0.09% (1/1132 anomalies), in case MDB196
5th toe hypoplasia 0.09% (1/1132 anomalies), in case MDB196
Bulbous nose 0.09% (1/1132 anomalies), in case MDB196
Hand clenching, fetal 0.09% (1/1132 anomalies), in case MDB196
Arachnodactyly 0.09% (1/1132 anomalies), in case MDB196
Short and dorsiflexed great toe 0.09% (1/1132 anomalies), in case MDB196
Abnormally aligned ribs 0.09% (1/1132 anomalies), in case MDB196
Recessed forehead 0.09% (1/1132 anomalies), in case MDB200
Double Outlet Right Ventricle, Without Transposition and VSD 0.09% (1/1132 anomalies), in case MDB201
Atrioventricular - channel 0.09% (1/1132 anomalies), in case MDB201
Cerebral cyst 0.09% (1/1132 anomalies), in case MDB201
Dilatation of the ascending aorta, congenital 0.09% (1/1132 anomalies), in case MDB208
Abnormal vertebral segmentation 0.09% (1/1132 anomalies), in case MDB208
Prostate hypoplasia 0.09% (1/1132 anomalies), in case MDB209
Pericardial effusion 0.09% (1/1132 anomalies), in case MDB209
Underdevelopment of the gyri. 0.09% (1/1132 anomalies), in case MDB210
Marginal subchorionic hematoma 0.09% (1/1132 anomalies), in case MDB219
Bowing of femur, congenital 0.09% (1/1132 anomalies), in case MDB223
Placental cysts 0.09% (1/1132 anomalies), in case MDB223
Dorsiflexion of foot, unilateral 0.09% (1/1132 anomalies), in case MDB224
Constriction Ring Deformity of the upper limbs 0.09% (1/1132 anomalies), in case MDB224
Congenital Hepatic Fibrosis, 0.09% (1/1132 anomalies), in case MDB231
Macrosomia 0.09% (1/1132 anomalies), in case MDB255
Bladder dilatation, fetal 0.09% (1/1132 anomalies), in case MDB255
Cloacal dysgenesis sequence (CDS) 0.09% (1/1132 anomalies), in case MDB255
Cleft palate, bilateral, complete 0.09% (1/1132 anomalies), in case MDB254
Renal hypertropy, fetal, bilateral 0.09% (1/1132 anomalies), in case MDB254
Acrocephaly 0.09% (1/1132 anomalies), in case MDB261
Absence of first finger, unilateral 0.09% (1/1132 anomalies), in case MDB263
Fissure of the upper gingiva, fetal 0.09% (1/1132 anomalies), in case MDB263
Vertebral hypoplasia, dorsolumbar 0.09% (1/1132 anomalies), in case MDB273
Diastrophic Dysplasia 0.09% (1/1132 anomalies), in case MDB274
Cubital deviation of the hand, bilateral 0.09% (1/1132 anomalies), in case MDB274
Spina bifida occulta, lombosacral 0.09% (1/1132 anomalies), in case MDB278
Inter-villous thrombosis 0.09% (1/1132 anomalies), in case MDB282
Incurvation of the ribs, bilateral 0.09% (1/1132 anomalies), in case MDB289
Femoral fracture, fetal, bilateral 0.09% (1/1132 anomalies), in case MDB289
Dextrocardia, isolated 0.09% (1/1132 anomalies), in case MDB293
Right ventricular hypoplasia 0.09% (1/1132 anomalies), in case MDB293
Left ventricular hypertrophy, 0.09% (1/1132 anomalies), in case MDB293
Thanatophoric dysplasia (Type I) 0.09% (1/1132 anomalies), in case MDB294
Stenosis of aqueduct of Sylvius 0.09% (1/1132 anomalies), in case MDB315
Pterygium colli 0.09% (1/1132 anomalies), in case MDB321
Pleural effusion, fetal 0.09% (1/1132 anomalies), in case MDB333
Renal hypoplasia, bilateral 0.09% (1/1132 anomalies), in case MDB339
Aglossia 0.09% (1/1132 anomalies), in case MDB358
Ureteral duplication, complete, unilateral 0.09% (1/1132 anomalies), in case MDB358
Dermoid cyst of the ovary 0.09% (1/1132 anomalies), in case MDB358
Malformed ear 0.09% (1/1132 anomalies), in case MDB359
Renal ectopia, simple 0.09% (1/1132 anomalies), in case MDB379
Cardiac hypoplasia, fetal 0.09% (1/1132 anomalies), in case MDB379
Absence of first fingers, bilateral 0.09% (1/1132 anomalies), in case MDB379
Laparoschisis 0.09% (1/1132 anomalies), in case MDB382
Anorchia, unilateral 0.09% (1/1132 anomalies), in case MDB382
Hypodactyly, hand, unilateral 0.09% (1/1132 anomalies), in case MDB382
Hepatic calcifications 0.09% (1/1132 anomalies), in case MDB414
Hypospadias, Penoscrotal 0.09% (1/1132 anomalies), in case MDB414
Arnold-Chiari Type II malformation (CM II) 0.09% (1/1132 anomalies), in case MDB417
Placental amniotic bands 0.09% (1/1132 anomalies), in case MDB425
Polydactyly of the foot 0.09% (1/1132 anomalies), in case MDB425
Holoprosencephaly 0.09% (1/1132 anomalies), in case MDB434
Craniofacial dysmorphism 0.09% (1/1132 anomalies), in case MDB434
Cleft lip, unilateral 0.09% (1/1132 anomalies), in case MDB452
Truncus bicaroticus 0.09% (1/1132 anomalies), in case MDB463
Single-nostril nose 0.09% (1/1132 anomalies), in case MDB463
Deep gray nuclear malformations(the caudate nuclei, thalami,..) 0.09% (1/1132 anomalies), in case MDB473
Incomplete cleavage of cerebral hemispheres 0.09% (1/1132 anomalies), in case MDB473
Myelomeningocele,thoracolumbar 0.09% (1/1132 anomalies), in case MDB473
hypoplasia of the rib 0.09% (1/1132 anomalies), in case MDB473
Pulmonary valve dysplasia 0.09% (1/1132 anomalies), in case MDB473
Tricuspid valve dysplasia 0.09% (1/1132 anomalies), in case MDB473
Clitoris hyperplasia 0.09% (1/1132 anomalies), in case MDB477
Encephalocele, frontal 0.09% (1/1132 anomalies), in case MDB483
Small mouth 0.09% (1/1132 anomalies), in case MDB483
Asplenia 0.09% (1/1132 anomalies), in case MDB483
Hypoplasia of the liver 0.09% (1/1132 anomalies), in case MDB483
Hypoplasia of the pancreas 0.09% (1/1132 anomalies), in case MDB483
rudimentary heart, congenital 0.09% (1/1132 anomalies), in case MDB483
Clavicle, absence of 0.09% (1/1132 anomalies), in case MDB483
small intestinal atresia and stenosis 0.09% (1/1132 anomalies), in case MDB483
Hypoplasia of diaphragm 0.09% (1/1132 anomalies), in case MDB491
Flexion contracture of upper limbs 0.09% (1/1132 anomalies), in case MDB503
Ureter agenesis, unilateral 0.09% (1/1132 anomalies), in case MDB503
Dysplastic kidney with tubular cysts 0.09% (1/1132 anomalies), in case MDB503
Cleft palate with cleft lip (CLP), median 0.09% (1/1132 anomalies), in case MDB504
Cutaneous bud 0.09% (1/1132 anomalies), in case MDB504
Aplasia cutis congenita, scalp 0.09% (1/1132 anomalies), in case MDB504
Pulmonary valve atresia 0.09% (1/1132 anomalies), in case MDB504
Right aortic arch 0.09% (1/1132 anomalies), in case MDB513
Partial agenesis of the corpus callosum (PACC) 0.09% (1/1132 anomalies), in case MDB520
Hypoplasia of the humerus, bilateral 0.09% (1/1132 anomalies), in case MDB522
Osteogenesis imperfecta 0.09% (1/1132 anomalies), in case MDB530
Short femur with angulated shaft 0.09% (1/1132 anomalies), in case MDB530
Radial deviation of the hand, unilateral 0.09% (1/1132 anomalies), in case MDB140
Transverse palmar crease, bilateral 0.09% (1/1132 anomalies), in case MDB199
Renal-hepatic-pancreatic dysplasia 0.09% (1/1132 anomalies), in case MDB213
Ureter hypoplasia 0.09% (1/1132 anomalies), in case MDB213
Abnormal canalicular pattern of pancreas 0.09% (1/1132 anomalies), in case MDB213
Rectovesical fistula 0.09% (1/1132 anomalies), in case MDB222
Amnion nodosum 0.09% (1/1132 anomalies), in case MDB222
Hypogenesis of pyramidal tracts 0.09% (1/1132 anomalies), in case MDB258
Glial heterotopia, multi-focal 0.09% (1/1132 anomalies), in case MDB258
Prominent upper lip 0.09% (1/1132 anomalies), in case MDB329
Hydromyelia 0.09% (1/1132 anomalies), in case MDB329
Micromelia, lower limb, unilateral 0.09% (1/1132 anomalies), in case MDB329
Pes cavus 0.09% (1/1132 anomalies), in case MDB48
Hydroureter, unilateral 0.09% (1/1132 anomalies), in case MDB250
Nuchal cord 0.09% (1/1132 anomalies), in case MDB250
Brachycephaly 0.09% (1/1132 anomalies), in case MDB268
Hypoplasia of optic nerve, bilateral 0.09% (1/1132 anomalies), in case MDB291
Arhinencephaly 0.09% (1/1132 anomalies), in case MDB291
Trigonocephaly 0.09% (1/1132 anomalies), in case MDB291
Absence of neocortex 0.09% (1/1132 anomalies), in case MDB291
Absence of the pyramid tracts, bilateral 0.09% (1/1132 anomalies), in case MDB291
Aberrant left subclavian artery 0.09% (1/1132 anomalies), in case MDB301
Lower limb hyperextension, Fetal 0.09% (1/1132 anomalies), in case MDB322
Gracile ribs 0.09% (1/1132 anomalies), in case MDB322
Cortical dysgenesis (CD), diffuse 0.09% (1/1132 anomalies), in case MDB322
Absence of neuron differentiation in the basal nuclei. 0.09% (1/1132 anomalies), in case MDB322
Renal pelvis dilatation, bilateral 0.09% (1/1132 anomalies), in case MDB320
Posterior urethral valves, congenital 0.09% (1/1132 anomalies), in case MDB320
Bladder wall thickness 0.09% (1/1132 anomalies), in case MDB320
Hypospadias, Glandular 0.09% (1/1132 anomalies), in case MDB320

Terminology and coding

References

No reference related to Placenta hypoplasia is available at the moment.

Last modified: 2008-12-12 14:30:48 by farideh

Created: 2008-02-19 00:00:00 by phsaw

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