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Clindodactyly of 5th finger, bilateral

DA: 48

Developmental anomaly information

Definition: Bilateral radio-volar deviation of little finger distal phalanx.

Developmental anomaly parent: (empty)	Topology: Human body > Limbs > Upper limbs > Hand > Fingers
System: Human body > musculoskeletal system. > Bones	Developmental anomaly category: Malformation

Case records MDB4, MDB23, MDB31, MDB48, MDB56, MDB61, MDB62, MDB69, MDB96, MDB111, MDB128, MDB132, MDB142, MDB145, MDB148, MDB149, MDB152, MDB196, MDB200, MDB215, MDB217, MDB219, MDB226, MDB233, MDB279, MDB315, MDB318, MDB331, MDB350, MDB362, MDB371, MDB387, MDB391, MDB481, MDB486, MDB487, MDB490, MDB514, MDB515, MDB535, MDB140, MDB167, MDB168, MDB319, MDB107, MDB324, MDB368

Links

Humpath: 13357

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

() in cases MDB, MDB, 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 :

Facial dysmorphism 5.08% (21/413 anomalies), in cases MDB48, MDB56, MDB96, MDB142, MDB145, MDB200, MDB215, MDB217, MDB226, MDB279, MDB315, MDB331, MDB350, MDB391, MDB481, MDB486, MDB487, MDB515, MDB168, MDB319, MDB107
Hypertelorism 4.6% (19/413 anomalies), in cases MDB31, MDB61, MDB69, MDB96, MDB128, MDB145, MDB148, MDB196, MDB215, MDB217, MDB315, MDB318, MDB331, MDB481, MDB486, MDB490, MDB514, MDB515, MDB368
Low-set ears 3.63% (15/413 anomalies), in cases MDB48, MDB69, MDB96, MDB196, MDB215, MDB217, MDB226, MDB331, MDB350, MDB362, MDB387, MDB515, MDB140, MDB168, MDB319
Pulmonary hypoplasia 2.66% (11/413 anomalies), in cases MDB23, MDB56, MDB69, MDB149, MDB200, MDB226, MDB391, MDB487, MDB168, MDB107, MDB324
Broad nasal bridge 2.66% (11/413 anomalies), in cases MDB31, MDB48, MDB132, MDB148, MDB149, MDB196, MDB215, MDB226, MDB318, MDB486, MDB107
Placenta hypoplasia 2.42% (10/413 anomalies), in cases MDB48, MDB56, MDB62, MDB196, MDB200, MDB215, MDB219, MDB315, MDB387, MDB140
Short neck 2.18% (9/413 anomalies), in cases MDB215, MDB331, MDB387, MDB486, MDB487, MDB514, MDB140, MDB319, MDB368
Intrauterine growth retardation, symmetric 2.18% (9/413 anomalies), in cases MDB215, MDB219, MDB387, MDB391, MDB481, MDB486, MDB140, MDB168, MDB368
Transverse palmar crease, bilateral 1.94% (8/413 anomalies), in cases MDB4, MDB132, MDB142, MDB362, MDB481, MDB515, MDB535, MDB368
Micrognathia 1.94% (8/413 anomalies), in cases MDB48, MDB145, MDB196, MDB200, MDB217, MDB315, MDB107, MDB324
Low nasal bridge 1.94% (8/413 anomalies), in cases MDB69, MDB145, MDB331, MDB350, MDB387, MDB515, MDB324, MDB368
Macroglossia 1.69% (7/413 anomalies), in cases MDB4, MDB145, MDB149, MDB200, MDB318, MDB514, MDB319
Neck edema 1.69% (7/413 anomalies), in cases MDB69, MDB149, MDB200, MDB279, MDB514, MDB324, MDB368
Wide space between 1st and 2nd toes, bilateral 1.69% (7/413 anomalies), in cases MDB96, MDB142, MDB149, MDB196, MDB233, MDB279, MDB107
Talipes equinovarus, bilateral 1.69% (7/413 anomalies), in cases MDB215, MDB219, MDB331, MDB362, MDB391, MDB140, MDB324
Retrognathia 1.69% (7/413 anomalies), in cases MDB279, MDB350, MDB391, MDB481, MDB487, MDB168, MDB368
Sloping forehead 1.45% (6/413 anomalies), in cases MDB69, MDB148, MDB200, MDB226, MDB279, MDB324
Adrenal hypoplasia, fetal 1.45% (6/413 anomalies), in cases MDB196, MDB371, MDB486, MDB487, MDB514, MDB168
Mongoloid slope of the palpebral fissures 1.21% (5/413 anomalies), in cases MDB61, MDB145, MDB149, MDB200, MDB515
Cerebral ventriculomegaly 1.21% (5/413 anomalies), in cases MDB69, MDB145, MDB217, MDB481, MDB490
Ventricular septal defect, muscular 0.97% (4/413 anomalies), in cases MDB4, MDB149, MDB391, MDB515
Epicanthus 0.97% (4/413 anomalies), in cases MDB23, MDB132, MDB200, MDB217
Single umblical artery (SUA)-Isolated 0.97% (4/413 anomalies), in cases MDB56, MDB215, MDB391, MDB487
Coarctation of aorta, 0.97% (4/413 anomalies), in cases MDB96, MDB142, MDB219, MDB391
Single transverse palmar crease, unilateral 0.97% (4/413 anomalies), in cases MDB128, MDB331, MDB387, MDB319
Right bilobate lung 0.97% (4/413 anomalies), in cases MDB145, MDB196, MDB215, MDB226
Narrow thorax 0.97% (4/413 anomalies), in cases MDB196, MDB486, MDB487, MDB514
Long philtrum 0.73% (3/413 anomalies), in cases MDB31, MDB486, MDB324
Lobulated, fused and horseshoe kidney 0.73% (3/413 anomalies), in cases MDB48, MDB391, MDB487
Hypogenesis of the Cerebellar Vermis 0.73% (3/413 anomalies), in cases MDB69, MDB490, MDB514
Nonimmune hydrops fetalis (NIHF) 0.73% (3/413 anomalies), in cases MDB111, MDB481, MDB168
Foot edema 0.73% (3/413 anomalies), in cases MDB132, MDB233, MDB514
Pulmonary artery hypoplasia 0.73% (3/413 anomalies), in cases MDB149, MDB481, MDB535
Rocker-bottom feet 0.73% (3/413 anomalies), in cases MDB196, MDB481, MDB515
Prominent and pointed nose 0.73% (3/413 anomalies), in cases MDB217, MDB391, MDB487
Corpus callosum agenesis 0.73% (3/413 anomalies), in cases MDB219, MDB481, MDB514
Toe hypoplasia, first, bilateral 0.73% (3/413 anomalies), in cases MDB350, MDB362, MDB368
Anencephaly 0.73% (3/413 anomalies), in cases MDB371, MDB486, MDB140
Exophthalmos, bilateral 0.73% (3/413 anomalies), in cases MDB371, MDB486, MDB140
Posteriorly inclined and low-positioned ears 0.73% (3/413 anomalies), in cases MDB481, MDB487, MDB324
Dilatation of ureter , bilateral, congenital 0.48% (2/413 anomalies), in cases MDB23, MDB324
Multicystic renal dysplasia,bilateral 0.48% (2/413 anomalies), in cases MDB23, MDB215
Renal pelvis dilatation, bilateral 0.48% (2/413 anomalies), in cases MDB23, MDB324
Defective developement of left ventricle 0.48% (2/413 anomalies), in cases MDB61, MDB111
Hypoplasia of ascending aorta 0.48% (2/413 anomalies), in cases MDB61, MDB111
Pulmonary artery dilatation, fetal 0.48% (2/413 anomalies), in cases MDB61, MDB111
Dolicocephaly 0.48% (2/413 anomalies), in cases MDB61, MDB481
Aortic valve atresia 0.48% (2/413 anomalies), in cases MDB61, MDB111
Macrocephaly 0.48% (2/413 anomalies), in cases MDB69, MDB217
Nasal hypoplasia 0.48% (2/413 anomalies), in cases MDB69, MDB200
Pterygium colli 0.48% (2/413 anomalies), in cases MDB69, MDB391
Hand edema 0.48% (2/413 anomalies), in cases MDB132, MDB514
Flat face 0.48% (2/413 anomalies), in cases MDB145, MDB318
Microretrognathia 0.48% (2/413 anomalies), in cases MDB148, MDB331
Flexion contracture of the fingers 0.48% (2/413 anomalies), in cases MDB148, MDB196
Tetralogy of Fallot 0.48% (2/413 anomalies), in cases MDB149, MDB535
Persistent Ductus arteriosus 0.48% (2/413 anomalies), in cases MDB149, MDB318
Frontal bossing 0.48% (2/413 anomalies), in cases MDB196, MDB318
Potter deformity sequence 0.48% (2/413 anomalies), in cases MDB219, MDB324
Potter's facies 0.48% (2/413 anomalies), in cases MDB219, MDB324
Cerebellar hypoplasia 0.48% (2/413 anomalies), in cases MDB315, MDB490
Ventricular septal defect, membranous 0.48% (2/413 anomalies), in cases MDB331, MDB387
Brachydactyly 0.48% (2/413 anomalies), in cases MDB362, MDB514
Anencephaly facies 0.48% (2/413 anomalies), in cases MDB371, MDB140
Cystic hygroma 0.48% (2/413 anomalies), in cases MDB391, MDB168
Preauricular hamartoma 0.48% (2/413 anomalies), in cases MDB391, MDB391
Cleft palate, bilateral 0.48% (2/413 anomalies), in cases MDB481, MDB168
Dextroposition of aorta 0.48% (2/413 anomalies), in cases MDB481, MDB535
Ureteral duplication, complete, unilateral 0.48% (2/413 anomalies), in cases MDB481, MDB487
Flattened nose 0.48% (2/413 anomalies), in cases MDB140, MDB324
Retroplacental hemorrhage 0.48% (2/413 anomalies), in cases MDB324, MDB368
Hypoplasia of the humerus, bilateral 0.24% (1/413 anomalies), in case MDB4
Hydronephrosis, congenital, bilateral 0.24% (1/413 anomalies), in case MDB23
Myelomeningocele,lumbosacral with hydrocephalus 0.24% (1/413 anomalies), in case MDB31
Beaked midbrain 0.24% (1/413 anomalies), in case MDB31
Tonsillar herniation of the cerebellum 0.24% (1/413 anomalies), in case MDB31
Arnold-Chiari Type II malformation (CM II) 0.24% (1/413 anomalies), in case MDB31
Pes cavus 0.24% (1/413 anomalies), in case MDB48
Diaphragmatic hernia, congenital 0.24% (1/413 anomalies), in case MDB56
cutaneous edema, fetal 0.24% (1/413 anomalies), in case MDB56
Absence of one paire the rib 0.24% (1/413 anomalies), in case MDB56
Dandy-Walker malformation 0.24% (1/413 anomalies), in case MDB69
Cleft lip, unilateral 0.24% (1/413 anomalies), in case MDB69
Syndactyly, simple (webbed), fingers 0.24% (1/413 anomalies), in case MDB69
Fingers amputation 0.24% (1/413 anomalies), in case MDB69
Holoprosencephaly 0.24% (1/413 anomalies), in case MDB69
Constriction Ring Deformity of the upper limbs 0.24% (1/413 anomalies), in case MDB69
Syndactyly of the toes, complex, bilateral 0.24% (1/413 anomalies), in case MDB69
Constriction Ring Deformity of the lower limbs 0.24% (1/413 anomalies), in case MDB69
Ring constriction deformity of the toes 0.24% (1/413 anomalies), in case MDB69
Toes amputation 0.24% (1/413 anomalies), in case MDB69
Nasal asymetria 0.24% (1/413 anomalies), in case MDB69
Gracile ribs 0.24% (1/413 anomalies), in case MDB69
Bowing of femur, congenital 0.24% (1/413 anomalies), in case MDB69
Left ventricular hypotrophy 0.24% (1/413 anomalies), in case MDB96
Right ventricle dilatation 0.24% (1/413 anomalies), in case MDB111
Aberrant right subclavian artery 0.24% (1/413 anomalies), in case MDB145
Overlapping fingers 0.24% (1/413 anomalies), in case MDB148
Meckel diverticulum 0.24% (1/413 anomalies), in case MDB148
hypoplasia of the rib 0.24% (1/413 anomalies), in case MDB148
Dilatation of the ascending aorta, congenital 0.24% (1/413 anomalies), in case MDB149
Patent Foramen Ovale 0.24% (1/413 anomalies), in case MDB149
Bicuspid pulmonary valve 0.24% (1/413 anomalies), in case MDB149
Arachnodactyly of the toes 0.24% (1/413 anomalies), in case MDB196
5th toe hypoplasia 0.24% (1/413 anomalies), in case MDB196
Relative Macrocephaly 0.24% (1/413 anomalies), in case MDB196
Bulbous nose 0.24% (1/413 anomalies), in case MDB196
Short philtrum 0.24% (1/413 anomalies), in case MDB196
Micropenis 0.24% (1/413 anomalies), in case MDB196
Intrauterine growth retardation, asymmetric 0.24% (1/413 anomalies), in case MDB196
Renal hypoplasia 0.24% (1/413 anomalies), in case MDB196
Hand clenching, fetal 0.24% (1/413 anomalies), in case MDB196
Arachnodactyly 0.24% (1/413 anomalies), in case MDB196
Short and dorsiflexed great toe 0.24% (1/413 anomalies), in case MDB196
Abnormally aligned ribs 0.24% (1/413 anomalies), in case MDB196
Syndactyly of the feet , simple (webbed), unilateral 0.24% (1/413 anomalies), in case MDB196
Recessed forehead 0.24% (1/413 anomalies), in case MDB200
Micromelia 0.24% (1/413 anomalies), in case MDB215
Cleft palate, median posterior 0.24% (1/413 anomalies), in case MDB215
Microphthalmia 0.24% (1/413 anomalies), in case MDB215
Unilobate lung, unilateral 0.24% (1/413 anomalies), in case MDB215
Hydrocephalus 0.24% (1/413 anomalies), in case MDB217
Prominence of nasofrontal angle 0.24% (1/413 anomalies), in case MDB217
Short umbilical cord 0.24% (1/413 anomalies), in case MDB219
Marginal subchorionic hematoma 0.24% (1/413 anomalies), in case MDB219
Polydactyly of the foot 0.24% (1/413 anomalies), in case MDB233
Wide space between 2nd and third toes,unilateral 0.24% (1/413 anomalies), in case MDB233
Hepatomegaly, fetal 0.24% (1/413 anomalies), in case MDB279
Stenosis of aqueduct of Sylvius 0.24% (1/413 anomalies), in case MDB315
Microcephaly 0.24% (1/413 anomalies), in case MDB315
Macrostomia 0.24% (1/413 anomalies), in case MDB315
Atrioventricular - channel 0.24% (1/413 anomalies), in case MDB318
Interauricular communication 0.24% (1/413 anomalies), in case MDB318
Polysplenia 0.24% (1/413 anomalies), in case MDB318
Brachycephaly 0.24% (1/413 anomalies), in case MDB331
Anotia 0.24% (1/413 anomalies), in case MDB391
Absence of diaphragm, left 0.24% (1/413 anomalies), in case MDB391
Dextrocardia, isolated 0.24% (1/413 anomalies), in case MDB391
Intestinal malrotation 0.24% (1/413 anomalies), in case MDB391
Pectus excavatum 0.24% (1/413 anomalies), in case MDB391
Ambiguous genitalia 0.24% (1/413 anomalies), in case MDB481
Imperforate Anus 0.24% (1/413 anomalies), in case MDB481
Persistent left superior vena cava 0.24% (1/413 anomalies), in case MDB481
Renal hypoplasia, unilateral 0.24% (1/413 anomalies), in case MDB481
Renal agenesis, unilateral 0.24% (1/413 anomalies), in case MDB481
Thymic hypoplasia 0.24% (1/413 anomalies), in case MDB481
Presence of an infantile uterus with both testes 0.24% (1/413 anomalies), in case MDB481
Absence of the Septum Pellucidum 0.24% (1/413 anomalies), in case MDB481
Probst bundle 0.24% (1/413 anomalies), in case MDB481
Omphalocele 0.24% (1/413 anomalies), in case MDB487
Large anterior fontanelle 0.24% (1/413 anomalies), in case MDB487
Trilobate lung, bilateral 0.24% (1/413 anomalies), in case MDB487
Splenic hypoplasia 0.24% (1/413 anomalies), in case MDB514
Right ventricular hypertrophy 0.24% (1/413 anomalies), in case MDB535
Thumb agenesis, unilateral 0.24% (1/413 anomalies), in case MDB140
Radial deviation of the hand, unilateral 0.24% (1/413 anomalies), in case MDB140
Myelomeningocele, lumbosacral 0.24% (1/413 anomalies), in case MDB167
Hypoplasia of the liver 0.24% (1/413 anomalies), in case MDB168
Hexadactyly, postaxial 0.24% (1/413 anomalies), in case MDB168
short nose 0.24% (1/413 anomalies), in case MDB319
Levocardia 0.24% (1/413 anomalies), in case MDB319
Small round skull 0.24% (1/413 anomalies), in case MDB107
Flattened occiput 0.24% (1/413 anomalies), in case MDB107
Trilobate lung, left 0.24% (1/413 anomalies), in case MDB107
Hypoplasia and dysplasia of the kidney, bilateral 0.24% (1/413 anomalies), in case MDB324
Megacystis 0.24% (1/413 anomalies), in case MDB324
Pericardial effusion 0.24% (1/413 anomalies), in case MDB324
Pleural effusion, fetal 0.24% (1/413 anomalies), in case MDB324
Ascites, fetal 0.24% (1/413 anomalies), in case MDB324

Terminology and coding

References

No reference related to Clindodactyly of 5th finger, bilateral is available at the moment.

Last modified: 2008-12-11 19:53:51 by farideh

Created: 2008-02-25 00:00:00 by phsaw

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