Malformations.org - View a developmental anomaly

Clindodactyly of 5th finger, unilateral

DA: 444

Developmental anomaly information

Definition: 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.	Developmental anomaly category: Malformation

Case records MDB22, MDB41, MDB120, MDB123, MDB131, MDB136, MDB139, MDB166, MDB216, MDB221, MDB224, MDB287, MDB300, MDB305, MDB367, MDB53, MDB518, MDB522, MDB146, MDB338, MDB147

Links

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

() in cases 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 :

Low-set ears 4.97% (9/181 anomalies), in cases MDB22, MDB136, MDB166, MDB216, MDB287, MDB53, MDB518, MDB522, MDB146
Placenta hypoplasia 4.97% (9/181 anomalies), in cases MDB22, MDB136, MDB139, MDB221, MDB224, MDB287, MDB305, MDB522, MDB338
Facial dysmorphism 4.97% (9/181 anomalies), in cases MDB136, MDB139, MDB166, MDB216, MDB367, MDB53, MDB518, MDB522, MDB338
Intrauterine growth retardation, symmetric 3.87% (7/181 anomalies), in cases MDB22, MDB136, MDB305, MDB367, MDB53, MDB522, MDB338
Hypertelorism 3.31% (6/181 anomalies), in cases MDB136, MDB139, MDB166, MDB367, MDB522, MDB338
Overlapping fingers 2.76% (5/181 anomalies), in cases MDB22, MDB120, MDB221, MDB224, MDB518
Pulmonary hypoplasia 2.21% (4/181 anomalies), in cases MDB22, MDB221, MDB367, MDB518
Retrognathia 2.21% (4/181 anomalies), in cases MDB136, MDB367, MDB518, MDB146
Wide space between 1st and 2nd toes, bilateral 2.21% (4/181 anomalies), in cases MDB216, MDB287, MDB305, MDB367
Low nasal bridge 2.21% (4/181 anomalies), in cases MDB287, MDB305, MDB146, MDB338
Triangular face 1.66% (3/181 anomalies), in cases MDB22, MDB53, MDB522
Single transverse palmar crease, unilateral 1.66% (3/181 anomalies), in cases MDB41, MDB136, MDB305
Coarctation of aorta, 1.66% (3/181 anomalies), in cases MDB136, MDB367, MDB53
Micrognathia 1.66% (3/181 anomalies), in cases MDB216, MDB287, MDB305
Microcephaly 1.1% (2/181 anomalies), in cases MDB22, MDB166
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 1.1% (2/181 anomalies), in cases MDB22, MDB22
Ventricular septal defect, muscular 1.1% (2/181 anomalies), in cases MDB22, MDB53
Meckel diverticulum 1.1% (2/181 anomalies), in cases MDB123, MDB136
Defective developement of left ventricle 1.1% (2/181 anomalies), in cases MDB136, MDB147
Corpus callosum agenesis 1.1% (2/181 anomalies), in cases MDB139, MDB166
Gastroschisis 1.1% (2/181 anomalies), in cases MDB166, MDB518
Fingers amputation 1.1% (2/181 anomalies), in cases MDB166, MDB224
Constriction Ring Deformity of the upper limbs 1.1% (2/181 anomalies), in cases MDB166, MDB224
Adrenal hypoplasia, fetal 1.1% (2/181 anomalies), in cases MDB221, MDB367
Syndactyly, simple (webbed), fingers 1.1% (2/181 anomalies), in cases MDB224, MDB53
Brachydactyly 1.1% (2/181 anomalies), in cases MDB287, MDB305
Long umbilical cord 1.1% (2/181 anomalies), in cases MDB300, MDB522
Short neck 1.1% (2/181 anomalies), in cases MDB367, MDB338
Renal pelvis dilatation, unilateral 1.1% (2/181 anomalies), in cases MDB53, MDB146
Omphalocele 0.55% (1/181 anomalies), in case MDB22
Persistent left superior vena cava 0.55% (1/181 anomalies), in case MDB22
Aberrant right subclavian artery 0.55% (1/181 anomalies), in case MDB22
Absence of innominate (brachiocephalic) vein 0.55% (1/181 anomalies), in case MDB22
Synophrys 0.55% (1/181 anomalies), in case MDB41
Macroglossia 0.55% (1/181 anomalies), in case MDB41
Pes cavus 0.55% (1/181 anomalies), in case MDB120
Metatarsus adductus 0.55% (1/181 anomalies), in case MDB120
Pulmonary artery dilatation, fetal 0.55% (1/181 anomalies), in case MDB136
Aortic valve stenosis, congenital 0.55% (1/181 anomalies), in case MDB136
Right ventricle dilatation 0.55% (1/181 anomalies), in case MDB136
Right atrium Enlargement 0.55% (1/181 anomalies), in case MDB136
Polydactyly of both fingers & toes, postaxial 0.55% (1/181 anomalies), in case MDB136
Intestinal malrotation 0.55% (1/181 anomalies), in case MDB136
Epicanthus 0.55% (1/181 anomalies), in case MDB139
Neuroepithelial cysts of the third ventricule,congenital 0.55% (1/181 anomalies), in case MDB139
Cleft palate with cleft lip (CLP), median 0.55% (1/181 anomalies), in case MDB166
Exencephaly 0.55% (1/181 anomalies), in case MDB166
Semilobar holoprosencephaly 0.55% (1/181 anomalies), in case MDB166
Optic nerve, absence of, bilateral 0.55% (1/181 anomalies), in case MDB166
Olfactory bulbs, absence of 0.55% (1/181 anomalies), in case MDB166
Cortical dysgenesis (CD), diffuse 0.55% (1/181 anomalies), in case MDB166
Absence of hippocampal commissure 0.55% (1/181 anomalies), in case MDB166
Badly-hemmed ears 0.55% (1/181 anomalies), in case MDB166
Prominent and pointed nose 0.55% (1/181 anomalies), in case MDB216
Cleft palate with cleft lip, unilateral, complete 0.55% (1/181 anomalies), in case MDB221
Dorsiflexion of foot, unilateral 0.55% (1/181 anomalies), in case MDB224
Talipes equinovarus,unilateral 0.55% (1/181 anomalies), in case MDB224
Hand edema 0.55% (1/181 anomalies), in case MDB224
Cubital deviation of the hand, unilateral 0.55% (1/181 anomalies), in case MDB224
Renal hypoplasia 0.55% (1/181 anomalies), in case MDB287
Muscular hypoplasia of the limbs 0.55% (1/181 anomalies), in case MDB300
Microstomia 0.55% (1/181 anomalies), in case MDB305
Diaphragmatic hernia,unilateral 0.55% (1/181 anomalies), in case MDB367
Dextrocardia, isolated 0.55% (1/181 anomalies), in case MDB367
Dilatation of the ascending aorta, congenital 0.55% (1/181 anomalies), in case MDB367
Neck edema 0.55% (1/181 anomalies), in case MDB367
Giant omphalocele 0.55% (1/181 anomalies), in case MDB53
Single umblical artery (SUA)-Isolated 0.55% (1/181 anomalies), in case MDB53
hypoplasia of the rib 0.55% (1/181 anomalies), in case MDB53
Lobulated, fused and horseshoe kidney 0.55% (1/181 anomalies), in case MDB53
Radial ray agenesis, unilateral 0.55% (1/181 anomalies), in case MDB53
Large anterior fontanelle 0.55% (1/181 anomalies), in case MDB53
Lumbosacral agenesis 0.55% (1/181 anomalies), in case MDB518
Relative Macrocephaly 0.55% (1/181 anomalies), in case MDB518
Narrow thorax 0.55% (1/181 anomalies), in case MDB518
Long philtrum 0.55% (1/181 anomalies), in case MDB518
Cleft palate, median posterior 0.55% (1/181 anomalies), in case MDB518
Renal agenesis, bilateral 0.55% (1/181 anomalies), in case MDB518
Agenesia of internal genital organs 0.55% (1/181 anomalies), in case MDB518
Thymic hypoplasia 0.55% (1/181 anomalies), in case MDB518
Persistent truncus arteriosus 0.55% (1/181 anomalies), in case MDB518
Right aortic arch 0.55% (1/181 anomalies), in case MDB518
Right bilobate lung 0.55% (1/181 anomalies), in case MDB518
Unilobate lung, unilateral 0.55% (1/181 anomalies), in case MDB518
Rachischisis 0.55% (1/181 anomalies), in case MDB518
Vertebral hypoplasia, dorsolumbar 0.55% (1/181 anomalies), in case MDB518
Rib deformation with abnormal numbers, bilateral 0.55% (1/181 anomalies), in case MDB518
Underdeveloped pelvic bones 0.55% (1/181 anomalies), in case MDB518
Hypoplasia of the humerus, bilateral 0.55% (1/181 anomalies), in case MDB522
Rocker-bottom feet 0.55% (1/181 anomalies), in case MDB522
Arthrogryposis 0.55% (1/181 anomalies), in case MDB522
Autosomal Recessive Polycystic Kidney Disease 0.55% (1/181 anomalies), in case MDB146
Ureteral duplication, complete, unilateral 0.55% (1/181 anomalies), in case MDB146
Nephromegaly, bilateral 0.55% (1/181 anomalies), in case MDB146
Renal-hepatic-pancreatic dysplasia 0.55% (1/181 anomalies), in case MDB146
Transverse palmar crease, bilateral 0.55% (1/181 anomalies), in case MDB146
Potter's facies 0.55% (1/181 anomalies), in case MDB146
Toe hypoplasia, first, bilateral 0.55% (1/181 anomalies), in case MDB146
Mongoloid slope of the palpebral fissures 0.55% (1/181 anomalies), in case MDB338
Talipes equinovarus, bilateral 0.55% (1/181 anomalies), in case MDB338
Mitral valve atresia 0.55% (1/181 anomalies), in case MDB147
Aortic atresia 0.55% (1/181 anomalies), in case MDB147
Patent Foramen Ovale 0.55% (1/181 anomalies), in case MDB147
Persistent Ductus arteriosus 0.55% (1/181 anomalies), in case MDB147
Fissure of the upper gingiva, fetal 0.55% (1/181 anomalies), in case MDB147
Periventricular Leukomalacia (PVL) 0.55% (1/181 anomalies), in case MDB147
Hydrocephalus 0.55% (1/181 anomalies), in case MDB147

Terminology and coding

References

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

Last modified: 2008-12-04 16:12:25 by farideh

Created: 2008-07-21 22:04:46 by farideh

<< Previous anomaly entry

Next anomaly entry >>