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Intrauterine growth retardation, symmetric

DA: 21

Developmental anomaly information

Definition: Intrauterine growth restriction describes poor growth of a fetus. Specifically, it refers to a fetus whose weight is below the 10th percentile for gestational age.

Synonyms:

IUGR
Fetal growth failure

Developmental anomaly parent: (empty)	Topology: Human body
System: Human body	Developmental anomaly category: Defect of growth (and organization) in early embryos

Case records MDB15, MDB18, MDB22, MDB53, MDB72, MDB79, MDB80, MDB86, MDB101, MDB103, MDB105, MDB115, MDB135, MDB136, MDB158, MDB162, MDB173, MDB190, MDB194, MDB199, MDB215, MDB219, MDB220, MDB223, MDB225, MDB234, MDB236, MDB237, MDB239, MDB245, MDB246, MDB249, MDB254, MDB256, MDB263, MDB265, MDB266, MDB274, MDB275, MDB277, MDB278, MDB284, MDB286, MDB291, MDB295, MDB305, MDB310, MDB314, MDB321, MDB322, MDB332, MDB337, MDB338, MDB340, MDB342, MDB343, MDB343, MDB339, MDB349, MDB358, MDB359, MDB367, MDB378, MDB380, MDB381, MDB387, MDB388, MDB389, MDB390, MDB391, MDB396, MDB399, MDB403, MDB404, MDB414, MDB418, MDB420, MDB422, MDB431, MDB433, MDB450, MDB452, MDB454, MDB458, MDB460, MDB465, MDB467, MDB471, MDB472, MDB473, MDB476, MDB477, MDB480, MDB481, MDB482, MDB483, MDB486, MDB489, MDB495, MDB512, MDB513, MDB520, MDB522, MDB140, MDB161, MDB164, MDB168, MDB235, MDB270, MDB302, MDB329, MDB11, MDB99, MDB368

Links

Humpath: 5011

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 :

Placenta hypoplasia 4.19% (44/1050 anomalies), in cases MDB15, MDB22, MDB86, MDB101, MDB103, MDB136, MDB162, MDB199, MDB215, MDB219, MDB223, MDB249, MDB254, MDB263, MDB266, MDB274, MDB275, MDB278, MDB286, MDB291, MDB305, MDB310, MDB321, MDB322, MDB332, MDB338, MDB339, MDB358, MDB359, MDB387, MDB396, MDB403, MDB414, MDB452, MDB471, MDB473, MDB477, MDB483, MDB495, MDB513, MDB520, MDB522, MDB140, MDB329
Facial dysmorphism 3.71% (39/1050 anomalies), in cases MDB53, MDB72, MDB101, MDB105, MDB115, MDB136, MDB215, MDB263, MDB266, MDB278, MDB286, MDB314, MDB321, MDB332, MDB338, MDB340, MDB339, MDB358, MDB359, MDB367, MDB378, MDB390, MDB391, MDB399, MDB418, MDB431, MDB452, MDB467, MDB471, MDB473, MDB480, MDB481, MDB486, MDB520, MDB522, MDB168, MDB270, MDB329, MDB11
Low-set ears 3.24% (34/1050 anomalies), in cases MDB22, MDB53, MDB72, MDB101, MDB103, MDB136, MDB162, MDB215, MDB223, MDB225, MDB249, MDB310, MDB321, MDB332, MDB343, MDB343, MDB339, MDB359, MDB380, MDB387, MDB390, MDB399, MDB404, MDB471, MDB473, MDB476, MDB483, MDB489, MDB520, MDB522, MDB140, MDB168, MDB270, MDB329
Pulmonary hypoplasia 3.24% (34/1050 anomalies), in cases MDB22, MDB103, MDB135, MDB223, MDB225, MDB236, MDB237, MDB246, MDB254, MDB266, MDB274, MDB275, MDB277, MDB291, MDB322, MDB337, MDB359, MDB367, MDB380, MDB381, MDB388, MDB389, MDB391, MDB404, MDB465, MDB471, MDB472, MDB477, MDB483, MDB495, MDB168, MDB302, MDB329, MDB11
Talipes equinovarus, bilateral 2.19% (23/1050 anomalies), in cases MDB79, MDB80, MDB103, MDB115, MDB158, MDB194, MDB215, MDB219, MDB223, MDB246, MDB254, MDB266, MDB274, MDB310, MDB322, MDB337, MDB338, MDB391, MDB396, MDB418, MDB431, MDB480, MDB140
Hypertelorism 2% (21/1050 anomalies), in cases MDB72, MDB105, MDB135, MDB136, MDB215, MDB239, MDB321, MDB322, MDB338, MDB358, MDB367, MDB450, MDB473, MDB480, MDB481, MDB486, MDB520, MDB522, MDB161, MDB270, MDB368
Retrognathia 1.71% (18/1050 anomalies), in cases MDB136, MDB265, MDB332, MDB339, MDB358, MDB359, MDB367, MDB391, MDB399, MDB431, MDB471, MDB472, MDB476, MDB481, MDB161, MDB168, MDB270, MDB368
Short neck 1.62% (17/1050 anomalies), in cases MDB215, MDB225, MDB322, MDB338, MDB343, MDB343, MDB367, MDB387, MDB403, MDB467, MDB476, MDB486, MDB140, MDB164, MDB270, MDB329, MDB368
Single umblical artery (SUA)-Isolated 1.52% (16/1050 anomalies), in cases MDB53, MDB105, MDB115, MDB173, MDB215, MDB246, MDB278, MDB322, MDB358, MDB359, MDB388, MDB391, MDB418, MDB420, MDB465, MDB99
Adrenal hypoplasia, fetal 1.52% (16/1050 anomalies), in cases MDB72, MDB286, MDB358, MDB367, MDB380, MDB403, MDB404, MDB450, MDB452, MDB454, MDB465, MDB477, MDB486, MDB520, MDB168, MDB302
Micrognathia 1.52% (16/1050 anomalies), in cases MDB101, MDB236, MDB263, MDB274, MDB286, MDB291, MDB305, MDB310, MDB314, MDB378, MDB380, MDB404, MDB467, MDB473, MDB489, MDB302
Nonimmune hydrops fetalis (NIHF) 1.33% (14/1050 anomalies), in cases MDB72, MDB135, MDB162, MDB225, MDB245, MDB337, MDB339, MDB481, MDB482, MDB483, MDB495, MDB512, MDB164, MDB168
Coarctation of aorta, 1.24% (13/1050 anomalies), in cases MDB53, MDB101, MDB105, MDB135, MDB136, MDB219, MDB225, MDB236, MDB286, MDB367, MDB391, MDB489, MDB302
Overlapping fingers 1.14% (12/1050 anomalies), in cases MDB15, MDB22, MDB101, MDB105, MDB158, MDB194, MDB322, MDB381, MDB399, MDB454, MDB489, MDB161
Triangular face 1.05% (11/1050 anomalies), in cases MDB22, MDB53, MDB223, MDB314, MDB332, MDB359, MDB390, MDB399, MDB431, MDB452, MDB522
Lobulated, fused and horseshoe kidney 1.05% (11/1050 anomalies), in cases MDB53, MDB101, MDB135, MDB265, MDB310, MDB332, MDB359, MDB380, MDB391, MDB399, MDB477
Ventricular septal defect, muscular 0.95% (10/1050 anomalies), in cases MDB22, MDB53, MDB101, MDB389, MDB390, MDB391, MDB399, MDB418, MDB452, MDB329
Toe hypoplasia, first, bilateral 0.95% (10/1050 anomalies), in cases MDB246, MDB254, MDB263, MDB310, MDB314, MDB414, MDB489, MDB161, MDB302, MDB368
Microcephaly 0.86% (9/1050 anomalies), in cases MDB15, MDB22, MDB220, MDB263, MDB291, MDB295, MDB322, MDB473, MDB329
Low nasal bridge 0.86% (9/1050 anomalies), in cases MDB103, MDB223, MDB305, MDB338, MDB387, MDB403, MDB471, MDB472, MDB368
Clindodactyly of 5th finger, bilateral 0.86% (9/1050 anomalies), in cases MDB215, MDB219, MDB387, MDB391, MDB481, MDB486, MDB140, MDB168, MDB368
Neck edema 0.86% (9/1050 anomalies), in cases MDB263, MDB310, MDB321, MDB322, MDB367, MDB404, MDB476, MDB520, MDB368
Cystic hygroma 0.76% (8/1050 anomalies), in cases MDB135, MDB225, MDB234, MDB337, MDB391, MDB495, MDB168, MDB329
Flattened nose 0.76% (8/1050 anomalies), in cases MDB223, MDB236, MDB239, MDB263, MDB450, MDB467, MDB140, MDB329
Exophthalmos, bilateral 0.76% (8/1050 anomalies), in cases MDB263, MDB286, MDB343, MDB343, MDB358, MDB480, MDB486, MDB140
Clindodactyly of 5th finger, unilateral 0.67% (7/1050 anomalies), in cases MDB22, MDB53, MDB136, MDB305, MDB338, MDB367, MDB522
Broad nasal bridge 0.67% (7/1050 anomalies), in cases MDB105, MDB135, MDB215, MDB321, MDB322, MDB486, MDB520
Single transverse palmar crease, unilateral 0.67% (7/1050 anomalies), in cases MDB136, MDB190, MDB305, MDB321, MDB387, MDB164, MDB270
Thalamic nuclei centrum medianum fusion 0.57% (6/1050 anomalies), in cases MDB18, MDB263, MDB291, MDB340, MDB161, MDB329
Potter deformity sequence 0.57% (6/1050 anomalies), in cases MDB80, MDB103, MDB219, MDB223, MDB450, MDB472
Microretrognathia 0.57% (6/1050 anomalies), in cases MDB103, MDB105, MDB223, MDB322, MDB403, MDB520
Rocker-bottom feet 0.57% (6/1050 anomalies), in cases MDB105, MDB194, MDB237, MDB450, MDB481, MDB522
Cleft palate, median posterior 0.57% (6/1050 anomalies), in cases MDB215, MDB337, MDB381, MDB431, MDB467, MDB513
Corpus callosum agenesis 0.57% (6/1050 anomalies), in cases MDB219, MDB263, MDB291, MDB473, MDB481, MDB329
Narrow thorax 0.57% (6/1050 anomalies), in cases MDB223, MDB286, MDB358, MDB467, MDB471, MDB486
Polydactyly of the hand, preaxial 0.57% (6/1050 anomalies), in cases MDB249, MDB322, MDB322, MDB380, MDB473, MDB513
Prominent and pointed nose 0.57% (6/1050 anomalies), in cases MDB286, MDB332, MDB378, MDB390, MDB391, MDB431
Ventricular septal defect, membranous 0.57% (6/1050 anomalies), in cases MDB310, MDB387, MDB388, MDB404, MDB420, MDB465
Long philtrum 0.57% (6/1050 anomalies), in cases MDB322, MDB378, MDB467, MDB486, MDB270, MDB329
Anencephaly 0.57% (6/1050 anomalies), in cases MDB343, MDB343, MDB381, MDB454, MDB486, MDB140
Cerebellar hypoplasia 0.48% (5/1050 anomalies), in cases MDB15, MDB291, MDB310, MDB340, MDB329
Cerebral ventriculomegaly 0.48% (5/1050 anomalies), in cases MDB15, MDB199, MDB234, MDB481, MDB520
Omphalocele 0.48% (5/1050 anomalies), in cases MDB22, MDB249, MDB277, MDB359, MDB420
Persistent left superior vena cava 0.48% (5/1050 anomalies), in cases MDB22, MDB105, MDB414, MDB418, MDB481
Large anterior fontanelle 0.48% (5/1050 anomalies), in cases MDB53, MDB414, MDB431, MDB471, MDB476
Macroglossia 0.48% (5/1050 anomalies), in cases MDB72, MDB343, MDB343, MDB433, MDB270
Pulmonary artery dilatation, fetal 0.48% (5/1050 anomalies), in cases MDB105, MDB135, MDB136, MDB332, MDB340
Myelomeningocele, lumbosacral 0.48% (5/1050 anomalies), in cases MDB194, MDB220, MDB245, MDB378, MDB396
Transverse palmar crease, bilateral 0.48% (5/1050 anomalies), in cases MDB199, MDB265, MDB481, MDB99, MDB368
Long umbilical cord 0.48% (5/1050 anomalies), in cases MDB236, MDB278, MDB291, MDB310, MDB522
Pulmonary artery hypoplasia 0.48% (5/1050 anomalies), in cases MDB246, MDB380, MDB418, MDB477, MDB481
Cleft palate, bilateral 0.48% (5/1050 anomalies), in cases MDB249, MDB332, MDB452, MDB481, MDB168
Triploidy, Maternal, nonmolar (triploidy by digyny) 0.48% (5/1050 anomalies), in cases MDB286, MDB332, MDB358, MDB380, MDB477
Arthrogryposis 0.48% (5/1050 anomalies), in cases MDB337, MDB450, MDB520, MDB522, MDB329
Renal agenesis, unilateral 0.38% (4/1050 anomalies), in cases MDB15, MDB358, MDB422, MDB481
Syndactyly, simple (webbed), fingers 0.38% (4/1050 anomalies), in cases MDB53, MDB72, MDB286, MDB337
Fingers amputation 0.38% (4/1050 anomalies), in cases MDB86, MDB277, MDB460, MDB512
Meckel diverticulum 0.38% (4/1050 anomalies), in cases MDB101, MDB136, MDB173, MDB11
Right atrium Enlargement 0.38% (4/1050 anomalies), in cases MDB105, MDB136, MDB246, MDB513
Intestinal malrotation 0.38% (4/1050 anomalies), in cases MDB136, MDB391, MDB399, MDB477
Potter's facies 0.38% (4/1050 anomalies), in cases MDB219, MDB223, MDB450, MDB472
Syndactyly of the fingers, complex, unilateral 0.38% (4/1050 anomalies), in cases MDB249, MDB286, MDB380, MDB302
Single cerebral ventricule 0.38% (4/1050 anomalies), in cases MDB263, MDB291, MDB340, MDB473
Wide space between 1st and 2nd toes, bilateral 0.38% (4/1050 anomalies), in cases MDB266, MDB305, MDB367, MDB302
Limbs hypoplasia 0.38% (4/1050 anomalies), in cases MDB274, MDB278, MDB471, MDB483
Hypogenesis of the Cerebellar Vermis 0.38% (4/1050 anomalies), in cases MDB278, MDB310, MDB359, MDB329
Olfactory bulbs, absence of 0.38% (4/1050 anomalies), in cases MDB291, MDB340, MDB480, MDB161
Olfactory nerve, absence of, bilateral 0.38% (4/1050 anomalies), in cases MDB291, MDB340, MDB480, MDB161
Cyclopia 0.29% (3/1050 anomalies), in cases MDB18, MDB291, MDB340
Polydactyly,of the hand, postaxial 0.29% (3/1050 anomalies), in cases MDB18, MDB340, MDB473
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.29% (3/1050 anomalies), in cases MDB22, MDB22, MDB173
Giant omphalocele 0.29% (3/1050 anomalies), in cases MDB53, MDB158, MDB473
Syndactyly of the feet , simple (webbed), unilateral 0.29% (3/1050 anomalies), in cases MDB101, MDB310, MDB322
Sloping forehead 0.29% (3/1050 anomalies), in cases MDB105, MDB322, MDB11
Imperforate Anus 0.29% (3/1050 anomalies), in cases MDB115, MDB246, MDB481
Foot edema 0.29% (3/1050 anomalies), in cases MDB162, MDB520, MDB164
Renal focal cystic dilatation of collecting tubules 0.29% (3/1050 anomalies), in cases MDB194, MDB275, MDB380
Multicystic renal dysplasia,bilateral 0.29% (3/1050 anomalies), in cases MDB215, MDB278, MDB418
Short umbilical cord 0.29% (3/1050 anomalies), in cases MDB219, MDB480, MDB483
Arnold-Chiari Type II malformation (CM II) 0.29% (3/1050 anomalies), in cases MDB220, MDB256, MDB378
Communicating hydrocephalus 0.29% (3/1050 anomalies), in cases MDB220, MDB234, MDB256
Cubital deviation of the hand, bilateral 0.29% (3/1050 anomalies), in cases MDB237, MDB274, MDB11
Limbs hypoplasia, lower extremities 0.29% (3/1050 anomalies), in cases MDB245, MDB378, MDB512
Holoprosencephaly, lobar 0.29% (3/1050 anomalies), in cases MDB263, MDB291, MDB329
Camptodactyly, bilateral 0.29% (3/1050 anomalies), in cases MDB266, MDB322, MDB396
Brachydactyly 0.29% (3/1050 anomalies), in cases MDB274, MDB305, MDB483
Placental amniotic bands 0.29% (3/1050 anomalies), in cases MDB277, MDB342, MDB460
Bladder hypoplasia 0.29% (3/1050 anomalies), in cases MDB278, MDB310, MDB418
Syndactyly of the toes, unilateral 0.29% (3/1050 anomalies), in cases MDB278, MDB380, MDB467
Arhinia 0.29% (3/1050 anomalies), in cases MDB291, MDB340, MDB480
Microstomia 0.29% (3/1050 anomalies), in cases MDB291, MDB305, MDB340
Trigonocephaly 0.29% (3/1050 anomalies), in cases MDB291, MDB340, MDB161
Syndactyly of the fingers, complex, bilateral 0.29% (3/1050 anomalies), in cases MDB332, MDB358, MDB477
Syndactyly of the toes, complex, bilateral 0.29% (3/1050 anomalies), in cases MDB332, MDB431, MDB477
Hydronephrosis, congenital, bilateral 0.29% (3/1050 anomalies), in cases MDB340, MDB489, MDB329
Dextrocardia, isolated 0.29% (3/1050 anomalies), in cases MDB367, MDB391, MDB418
Anencephaly facies 0.29% (3/1050 anomalies), in cases MDB381, MDB454, MDB140
Ambiguous genitalia 0.29% (3/1050 anomalies), in cases MDB414, MDB477, MDB481
Right aortic arch 0.29% (3/1050 anomalies), in cases MDB418, MDB513, MDB235
Thymic hypoplasia 0.29% (3/1050 anomalies), in cases MDB481, MDB483, MDB513
Microtia 0.19% (2/1050 anomalies), in cases MDB15, MDB467
Cleft palate with cleft lip, unilateral, complete 0.19% (2/1050 anomalies), in cases MDB15, MDB86
Cortical dysgenesis (CD), diffuse 0.19% (2/1050 anomalies), in cases MDB18, MDB322
Holoprosencephaly, alobar 0.19% (2/1050 anomalies), in cases MDB18, MDB340
Proboscis 0.19% (2/1050 anomalies), in cases MDB18, MDB340
Aberrant right subclavian artery 0.19% (2/1050 anomalies), in cases MDB22, MDB404
hypoplasia of the rib 0.19% (2/1050 anomalies), in cases MDB53, MDB473
Renal pelvis dilatation, unilateral 0.19% (2/1050 anomalies), in cases MDB53, MDB321
Radial ray agenesis, unilateral 0.19% (2/1050 anomalies), in cases MDB53, MDB431
Cubital deviation of the hand, unilateral 0.19% (2/1050 anomalies), in cases MDB80, MDB239
Gastroschisis 0.19% (2/1050 anomalies), in cases MDB86, MDB480
Scoliosis, congenital 0.19% (2/1050 anomalies), in cases MDB86, MDB105
Aortic valve atresia 0.19% (2/1050 anomalies), in cases MDB101, MDB332
Placenta circumvallata 0.19% (2/1050 anomalies), in cases MDB103, MDB256
Gracile ribs 0.19% (2/1050 anomalies), in cases MDB105, MDB322
Right ventricular hypoplasia 0.19% (2/1050 anomalies), in cases MDB105, MDB246
Aortic valve stenosis, congenital 0.19% (2/1050 anomalies), in cases MDB105, MDB136
Hypoplasia of ascending aorta 0.19% (2/1050 anomalies), in cases MDB105, MDB340
Right bilobate lung 0.19% (2/1050 anomalies), in cases MDB105, MDB215
Cleft palate, bilateral, complete 0.19% (2/1050 anomalies), in cases MDB105, MDB254
Thumb agenesis, unilateral 0.19% (2/1050 anomalies), in cases MDB115, MDB140
Crossed fused renal ectopia 0.19% (2/1050 anomalies), in cases MDB115, MDB173
Hand edema 0.19% (2/1050 anomalies), in cases MDB135, MDB162
Transverse aortic hypoplasia 0.19% (2/1050 anomalies), in cases MDB135, MDB495
Defective developement of left ventricle 0.19% (2/1050 anomalies), in cases MDB136, MDB340
Nephromegaly, bilateral 0.19% (2/1050 anomalies), in cases MDB194, MDB278
Micromelia 0.19% (2/1050 anomalies), in cases MDB215, MDB266
Frontal bossing 0.19% (2/1050 anomalies), in cases MDB223, MDB471
Placental hypermaturity 0.19% (2/1050 anomalies), in cases MDB234, MDB332
Infarcted placenta 0.19% (2/1050 anomalies), in cases MDB236, MDB450
Renal hypoplasia 0.19% (2/1050 anomalies), in cases MDB246, MDB458
Arthrogryposis,lower limbs 0.19% (2/1050 anomalies), in cases MDB249, MDB275
Osteogenesis imperfecta, Type II 0.19% (2/1050 anomalies), in cases MDB254, MDB266
Decreased skull bone mineralization 0.19% (2/1050 anomalies), in cases MDB254, MDB266
Nasal hypoplasia 0.19% (2/1050 anomalies), in cases MDB263, MDB483
Gothic palate 0.19% (2/1050 anomalies), in cases MDB263, MDB322
Thumb agenesis, bilateral 0.19% (2/1050 anomalies), in cases MDB265, MDB422
absence of radius, bilateral 0.19% (2/1050 anomalies), in cases MDB265, MDB284
Ulna,absence of, bilateral 0.19% (2/1050 anomalies), in cases MDB265, MDB284
Bowing of long bones 0.19% (2/1050 anomalies), in cases MDB266, MDB274
Camptodactyly, unilateral 0.19% (2/1050 anomalies), in cases MDB275, MDB278
Semilobar holoprosencephaly 0.19% (2/1050 anomalies), in cases MDB277, MDB473
Retroplacental hemorrhage 0.19% (2/1050 anomalies), in cases MDB277, MDB368
Enophtalmus 0.19% (2/1050 anomalies), in cases MDB277, MDB11
Cleft palate with cleft lip,bilateral, complete 0.19% (2/1050 anomalies), in cases MDB277, MDB418
Arhinencephaly 0.19% (2/1050 anomalies), in cases MDB291, MDB480
Anophthalmos, bilateral 0.19% (2/1050 anomalies), in cases MDB291, MDB480
Pterygium colli 0.19% (2/1050 anomalies), in cases MDB321, MDB391
Hexadactyly, postaxial 0.19% (2/1050 anomalies), in cases MDB321, MDB168
Wide space between 1st and 2nd toes, unilateral 0.19% (2/1050 anomalies), in cases MDB322, MDB414
Bicornuate uterus 0.19% (2/1050 anomalies), in cases MDB340, MDB458
Rachischisis, cervical 0.19% (2/1050 anomalies), in cases MDB343, MDB343
Narrow palate 0.19% (2/1050 anomalies), in cases MDB343, MDB343
Ureteral duplication, complete, unilateral 0.19% (2/1050 anomalies), in cases MDB358, MDB481
Malformed ear 0.19% (2/1050 anomalies), in cases MDB359, MDB431
Renal pelvis dilatation, bilateral 0.19% (2/1050 anomalies), in cases MDB388, MDB489
Dilatation of ureter , bilateral, congenital 0.19% (2/1050 anomalies), in cases MDB388, MDB329
Anotia 0.19% (2/1050 anomalies), in cases MDB391, MDB467
Absence of diaphragm, left 0.19% (2/1050 anomalies), in cases MDB391, MDB483
Preauricular hamartoma 0.19% (2/1050 anomalies), in cases MDB391, MDB391
Relative Macrocephaly 0.19% (2/1050 anomalies), in cases MDB414, MDB477
Hepatic calcifications 0.19% (2/1050 anomalies), in cases MDB414, MDB450
Posteriorly inclined and low-positioned ears 0.19% (2/1050 anomalies), in cases MDB418, MDB481
Palpebral edema, bilateral 0.19% (2/1050 anomalies), in cases MDB450, MDB472
Dolicocephaly 0.19% (2/1050 anomalies), in cases MDB472, MDB481
Teratoma, cerebral 0.19% (2/1050 anomalies), in cases MDB480, MDB480
Dextroposition of aorta 0.19% (2/1050 anomalies), in cases MDB481, MDB513
Asplenia 0.19% (2/1050 anomalies), in cases MDB483, MDB11
Hypoplasia of the liver 0.19% (2/1050 anomalies), in cases MDB483, MDB168
Tetralogy of Fallot 0.19% (2/1050 anomalies), in cases MDB513, MDB235
Polymicrogyria, focal 0.19% (2/1050 anomalies), in cases MDB329, MDB329
Micropenis 0.1% (1/1050 anomalies), in case MDB18
Absence of innominate (brachiocephalic) vein 0.1% (1/1050 anomalies), in case MDB22
Incomplete and partial hydatidiform mole 0.1% (1/1050 anomalies), in case MDB72
Diandric triploidy 0.1% (1/1050 anomalies), in case MDB72
Pes cavus 0.1% (1/1050 anomalies), in case MDB72
Cleft lip 0.1% (1/1050 anomalies), in case MDB72
Flexion contracture of upper limbs 0.1% (1/1050 anomalies), in case MDB79
Encephalocele 0.1% (1/1050 anomalies), in case MDB86
Shortening (micromelia) of upper limb(s), unilateral 0.1% (1/1050 anomalies), in case MDB86
Pulmonary Cysts, congenital 0.1% (1/1050 anomalies), in case MDB86
Syndactyly of the feet , simple (webbed), bilateral 0.1% (1/1050 anomalies), in case MDB101
Turned-up nose 0.1% (1/1050 anomalies), in case MDB101
Bone mineralization defect 0.1% (1/1050 anomalies), in case MDB103
Cubital pterygium, bilateral 0.1% (1/1050 anomalies), in case MDB105
Axillary pterygia,unilateral 0.1% (1/1050 anomalies), in case MDB105
Aortic isthmus stenosis 0.1% (1/1050 anomalies), in case MDB105
Platyspondyly 0.1% (1/1050 anomalies), in case MDB105
snub-nosed 0.1% (1/1050 anomalies), in case MDB105
Polyhydramnios 0.1% (1/1050 anomalies), in case MDB105
dextro-Transposition of the great arteries 0.1% (1/1050 anomalies), in case MDB105
Constriction Ring Deformity of the upper limbs 0.1% (1/1050 anomalies), in case MDB115
Encephalocele, parietal 0.1% (1/1050 anomalies), in case MDB115
Ascites, fetal 0.1% (1/1050 anomalies), in case MDB135
Epicanthus 0.1% (1/1050 anomalies), in case MDB135
Pleural effusion, fetal 0.1% (1/1050 anomalies), in case MDB135
Right ventricle dilatation 0.1% (1/1050 anomalies), in case MDB136
Polydactyly of both fingers & toes, postaxial 0.1% (1/1050 anomalies), in case MDB136
Hypoplasia of the humerus, unilateral 0.1% (1/1050 anomalies), in case MDB173
Split-hand/split-foot malformation (SHFM) 0.1% (1/1050 anomalies), in case MDB173
Ovarian hypoplasia, unilateral 0.1% (1/1050 anomalies), in case MDB173
fallopian tube dysgenesis 0.1% (1/1050 anomalies), in case MDB173
genital ambiguity 0.1% (1/1050 anomalies), in case MDB173
Uterus agenesis 0.1% (1/1050 anomalies), in case MDB173
Microphthalmia 0.1% (1/1050 anomalies), in case MDB215
Unilobate lung, unilateral 0.1% (1/1050 anomalies), in case MDB215
Marginal subchorionic hematoma 0.1% (1/1050 anomalies), in case MDB219
Tonsillar herniation of the cerebellum 0.1% (1/1050 anomalies), in case MDB220
Bowing of femur, congenital 0.1% (1/1050 anomalies), in case MDB223
Placental cysts 0.1% (1/1050 anomalies), in case MDB223
Recessed forehead 0.1% (1/1050 anomalies), in case MDB239
Low-set ear, unilateral 0.1% (1/1050 anomalies), in case MDB239
Shortening (micromelia) of upper limb(s) 0.1% (1/1050 anomalies), in case MDB246
Amelia of the upper limb, unilateral 0.1% (1/1050 anomalies), in case MDB246
Dysplasia of hip, unilateral, congenital 0.1% (1/1050 anomalies), in case MDB246
Scrotal hypoplasia 0.1% (1/1050 anomalies), in case MDB246
Renal hypertropy, fetal, bilateral 0.1% (1/1050 anomalies), in case MDB254
Myelomeningocele,lumbosacral with hydrocephalus 0.1% (1/1050 anomalies), in case MDB256
Absence of first finger, unilateral 0.1% (1/1050 anomalies), in case MDB263
Fissure of the upper gingiva, fetal 0.1% (1/1050 anomalies), in case MDB263
Diastrophic Dysplasia 0.1% (1/1050 anomalies), in case MDB274
Prominent infraorbital creases 0.1% (1/1050 anomalies), in case MDB277
Ectopia cordis 0.1% (1/1050 anomalies), in case MDB277
Exencephaly 0.1% (1/1050 anomalies), in case MDB277
Congenital Muscular Torticollis, Fetal 0.1% (1/1050 anomalies), in case MDB277
Diaphragmatic hernia, congenital 0.1% (1/1050 anomalies), in case MDB277
Spina bifida occulta, lombosacral 0.1% (1/1050 anomalies), in case MDB278
Amelia of the upper limbs, bilateral 0.1% (1/1050 anomalies), in case MDB284
Absence of humerus, bilateral, congenital 0.1% (1/1050 anomalies), in case MDB284
Hypoplasia of optic nerve, bilateral 0.1% (1/1050 anomalies), in case MDB291
Absence of neocortex 0.1% (1/1050 anomalies), in case MDB291
Absence of the pyramid tracts, bilateral 0.1% (1/1050 anomalies), in case MDB291
Splenomegaly, congenital 0.1% (1/1050 anomalies), in case MDB295
Circummarginate Placenta 0.1% (1/1050 anomalies), in case MDB295
Lower limb hyperextension, Fetal 0.1% (1/1050 anomalies), in case MDB322
Polysplenia 0.1% (1/1050 anomalies), in case MDB322
Scoliosis, dextroconvex, thoracic 0.1% (1/1050 anomalies), in case MDB322
Neuronal migration anomaly 0.1% (1/1050 anomalies), in case MDB322
Hydrocephalus 0.1% (1/1050 anomalies), in case MDB322
Absence of neuron differentiation in the basal nuclei. 0.1% (1/1050 anomalies), in case MDB322
Flexion contracture of the fingers 0.1% (1/1050 anomalies), in case MDB322
Small round skull 0.1% (1/1050 anomalies), in case MDB322
Pectus carinatum 0.1% (1/1050 anomalies), in case MDB337
Periventricular Leukomalacia (PVL) 0.1% (1/1050 anomalies), in case MDB337
Mongoloid slope of the palpebral fissures 0.1% (1/1050 anomalies), in case MDB338
Hypoplastic left heart syndrome (HLHS) 0.1% (1/1050 anomalies), in case MDB340
Hypoplasia of the aortic isthmus 0.1% (1/1050 anomalies), in case MDB340
Mitral valve stenosis 0.1% (1/1050 anomalies), in case MDB340
Optic nerve, absence of, bilateral 0.1% (1/1050 anomalies), in case MDB340
Pachygyria 0.1% (1/1050 anomalies), in case MDB340
Transverse amputation of limb 0.1% (1/1050 anomalies), in case MDB342
overlapping skull bones 0.1% (1/1050 anomalies), in case MDB342
Renal hypoplasia, bilateral 0.1% (1/1050 anomalies), in case MDB339
Macrocephaly 0.1% (1/1050 anomalies), in case MDB358
Aglossia 0.1% (1/1050 anomalies), in case MDB358
Unilobate lung, bilateral 0.1% (1/1050 anomalies), in case MDB358
Dermoid cyst of the ovary 0.1% (1/1050 anomalies), in case MDB358
Diaphragmatic hernia,unilateral 0.1% (1/1050 anomalies), in case MDB367
Dilatation of the ascending aorta, congenital 0.1% (1/1050 anomalies), in case MDB367
Thin upper lip 0.1% (1/1050 anomalies), in case MDB378
Toe hypoplasia, unilateral 0.1% (1/1050 anomalies), in case MDB380
Axillary pterygia, bilateral 0.1% (1/1050 anomalies), in case MDB381
Arachnodactyly 0.1% (1/1050 anomalies), in case MDB381
Large thorax 0.1% (1/1050 anomalies), in case MDB381
Prominent shoulder 0.1% (1/1050 anomalies), in case MDB381
Narrow pelvis 0.1% (1/1050 anomalies), in case MDB381
Flat abdomen 0.1% (1/1050 anomalies), in case MDB381
Holoanencephaly 0.1% (1/1050 anomalies), in case MDB381
Pectus excavatum 0.1% (1/1050 anomalies), in case MDB391
left carotid artery, aberrant 0.1% (1/1050 anomalies), in case MDB404
Hypospadias, Penoscrotal 0.1% (1/1050 anomalies), in case MDB414
Ureter hypoplasia 0.1% (1/1050 anomalies), in case MDB418
Unicorn Uterus 0.1% (1/1050 anomalies), in case MDB418
Fallopian tube, absence of 0.1% (1/1050 anomalies), in case MDB418
Trilobate lung, bilateral 0.1% (1/1050 anomalies), in case MDB420
Radial clubhand 0.1% (1/1050 anomalies), in case MDB422
Duodenal atresia and stenosis, congenital 0.1% (1/1050 anomalies), in case MDB422
Intestinal dilatation, congenital 0.1% (1/1050 anomalies), in case MDB422
Radial ray agenesis, bilateral 0.1% (1/1050 anomalies), in case MDB422
Multicystic renal dysplasia, unilateral 0.1% (1/1050 anomalies), in case MDB422
Thumb hypoplasia,unilateral 0.1% (1/1050 anomalies), in case MDB431
Wide space between 2nd and third fingers 0.1% (1/1050 anomalies), in case MDB431
Dislocation of hip, unilateral 0.1% (1/1050 anomalies), in case MDB431
Scaphoid abdomen 0.1% (1/1050 anomalies), in case MDB431
Badly-hemmed ears 0.1% (1/1050 anomalies), in case MDB450
Cleft lip, unilateral 0.1% (1/1050 anomalies), in case MDB452
Persistent truncus arteriosus 0.1% (1/1050 anomalies), in case MDB452
Absence of skull bones 0.1% (1/1050 anomalies), in case MDB454
Turricephaly 0.1% (1/1050 anomalies), in case MDB458
Renal ectopia,crossed 0.1% (1/1050 anomalies), in case MDB458
Interhemispheric cyst, brain 0.1% (1/1050 anomalies), in case MDB458
Ureter hypoplaia, unilateral 0.1% (1/1050 anomalies), in case MDB458
Toes amputation 0.1% (1/1050 anomalies), in case MDB460
Otopaladigital syndrome, Type II; 0.1% (1/1050 anomalies), in case MDB467
Tetra-amelia 0.1% (1/1050 anomalies), in case MDB467
Polydactyly postaxial & preaxial of toes 0.1% (1/1050 anomalies), in case MDB467
Thumb malformation & mal-implanted 0.1% (1/1050 anomalies), in case MDB467
Choanal Atresia 0.1% (1/1050 anomalies), in case MDB467
Flat face 0.1% (1/1050 anomalies), in case MDB472
Oligohydramnios 0.1% (1/1050 anomalies), in case MDB472
Deep gray nuclear malformations(the caudate nuclei, thalami,..) 0.1% (1/1050 anomalies), in case MDB473
Incomplete cleavage of cerebral hemispheres 0.1% (1/1050 anomalies), in case MDB473
Short philtrum 0.1% (1/1050 anomalies), in case MDB473
Myelomeningocele,thoracolumbar 0.1% (1/1050 anomalies), in case MDB473
Pulmonary valve dysplasia 0.1% (1/1050 anomalies), in case MDB473
Tricuspid valve dysplasia 0.1% (1/1050 anomalies), in case MDB473
Interauricular communication 0.1% (1/1050 anomalies), in case MDB473
Pulmonary lobation anomalies 0.1% (1/1050 anomalies), in case MDB477
Clitoris hyperplasia 0.1% (1/1050 anomalies), in case MDB477
Limb-body-wall complex syndrome 0.1% (1/1050 anomalies), in case MDB480
Primordial iris 0.1% (1/1050 anomalies), in case MDB480
Clivus, absence of 0.1% (1/1050 anomalies), in case MDB480
Posterior cranial fossa dismorphisme 0.1% (1/1050 anomalies), in case MDB480
Rudimentary radius and ulna (unilateral) 0.1% (1/1050 anomalies), in case MDB480
Oligodactyly 0.1% (1/1050 anomalies), in case MDB480
Renal hypoplasia, unilateral 0.1% (1/1050 anomalies), in case MDB481
Presence of an infantile uterus with both testes 0.1% (1/1050 anomalies), in case MDB481
Absence of the Septum Pellucidum 0.1% (1/1050 anomalies), in case MDB481
Probst bundle 0.1% (1/1050 anomalies), in case MDB481
Sever pale fetus 0.1% (1/1050 anomalies), in case MDB482
Acardiac twinning, with pump twin demise 0.1% (1/1050 anomalies), in case MDB482
Encephalocele, frontal 0.1% (1/1050 anomalies), in case MDB483
Small mouth 0.1% (1/1050 anomalies), in case MDB483
Hypoplasia of the pancreas 0.1% (1/1050 anomalies), in case MDB483
rudimentary heart, congenital 0.1% (1/1050 anomalies), in case MDB483
Absence of one paire the rib 0.1% (1/1050 anomalies), in case MDB483
Clavicle, absence of 0.1% (1/1050 anomalies), in case MDB483
small intestinal atresia and stenosis 0.1% (1/1050 anomalies), in case MDB483
Ureterovesical junction stenosis 0.1% (1/1050 anomalies), in case MDB489
Constriction Ring Deformity of the lower limbs 0.1% (1/1050 anomalies), in case MDB512
Brachydactyly of the toes 0.1% (1/1050 anomalies), in case MDB512
Right ventricular hypertrophy 0.1% (1/1050 anomalies), in case MDB513
Pulmonary valve hypoplasia, congenital 0.1% (1/1050 anomalies), in case MDB513
Partial agenesis of the corpus callosum (PACC) 0.1% (1/1050 anomalies), in case MDB520
Hypoplasia of the humerus, bilateral 0.1% (1/1050 anomalies), in case MDB522
Radial deviation of the hand, unilateral 0.1% (1/1050 anomalies), in case MDB140
Holoprosencephaly 0.1% (1/1050 anomalies), in case MDB161
Megacystis 0.1% (1/1050 anomalies), in case MDB329
Prominent upper lip 0.1% (1/1050 anomalies), in case MDB329
Hydromyelia 0.1% (1/1050 anomalies), in case MDB329
Micromelia, lower limb, unilateral 0.1% (1/1050 anomalies), in case MDB329
Palpebral hypoplasia 0.1% (1/1050 anomalies), in case MDB11
Prognathism, maxillary 0.1% (1/1050 anomalies), in case MDB11
Frontal bone hypoplasia 0.1% (1/1050 anomalies), in case MDB11
Relative Microcephaly 0.1% (1/1050 anomalies), in case MDB11

Terminology and coding

References

No reference related to Intrauterine growth retardation, symmetric is available at the moment.

Last modified: 2008-12-16 20:06:34 by farideh

Created: 2008-02-15 00:00:00 by phsaw

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