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Overlapping fingers

DA: 9

Developmental anomaly information

Definition: Finger terminal phalanx malunion.

Synonyms:

Finger overlap

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

Case records MDB120, MDB15, MDB22, MDB73, MDB88, MDB91, MDB100, MDB101, MDB105, MDB143, MDB148, MDB155, MDB157, MDB175, MDB179, MDB194, MDB201, MDB238, MDB221, MDB224, MDB322, MDB381, MDB399, MDB454, MDB489, MDB518, MDB158, MDB161

Links

Humpath: 8459

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 :

Intrauterine growth retardation, symmetric 4.17% (12/288 anomalies), in cases MDB15, MDB22, MDB101, MDB105, MDB194, MDB322, MDB381, MDB399, MDB454, MDB489, MDB158, MDB161
Placenta hypoplasia 3.47% (10/288 anomalies), in cases MDB15, MDB22, MDB91, MDB100, MDB101, MDB157, MDB201, MDB221, MDB224, MDB322
Pulmonary hypoplasia 3.47% (10/288 anomalies), in cases MDB22, MDB100, MDB155, MDB175, MDB201, MDB238, MDB221, MDB322, MDB381, MDB518
Low-set ears 3.13% (9/288 anomalies), in cases MDB22, MDB100, MDB101, MDB175, MDB201, MDB238, MDB399, MDB489, MDB518
Talipes equinovarus, bilateral 2.08% (6/288 anomalies), in cases MDB88, MDB143, MDB194, MDB238, MDB322, MDB158
Facial dysmorphism 2.08% (6/288 anomalies), in cases MDB100, MDB101, MDB105, MDB238, MDB399, MDB518
Hypertelorism 2.08% (6/288 anomalies), in cases MDB100, MDB105, MDB148, MDB238, MDB322, MDB161
Clindodactyly of 5th finger, unilateral 1.74% (5/288 anomalies), in cases MDB120, MDB22, MDB221, MDB224, MDB518
Microcephaly 1.39% (4/288 anomalies), in cases MDB15, MDB22, MDB175, MDB322
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 1.39% (4/288 anomalies), in cases MDB22, MDB22, MDB155, MDB179
Ventricular septal defect, muscular 1.39% (4/288 anomalies), in cases MDB22, MDB101, MDB157, MDB399
Broad nasal bridge 1.39% (4/288 anomalies), in cases MDB100, MDB105, MDB148, MDB322
Retrognathia 1.39% (4/288 anomalies), in cases MDB100, MDB399, MDB518, MDB161
Coarctation of aorta, 1.39% (4/288 anomalies), in cases MDB101, MDB105, MDB157, MDB489
Meckel diverticulum 1.39% (4/288 anomalies), in cases MDB101, MDB148, MDB157, MDB179
Micrognathia 1.39% (4/288 anomalies), in cases MDB101, MDB157, MDB238, MDB489
Sloping forehead 1.39% (4/288 anomalies), in cases MDB105, MDB148, MDB201, MDB322
Microretrognathia 1.39% (4/288 anomalies), in cases MDB105, MDB148, MDB201, MDB322
Single umblical artery (SUA)-Isolated 1.39% (4/288 anomalies), in cases MDB105, MDB155, MDB179, MDB322
Adrenal hypoplasia, fetal 1.39% (4/288 anomalies), in cases MDB175, MDB201, MDB221, MDB454
Triangular face 1.04% (3/288 anomalies), in cases MDB22, MDB201, MDB399
Omphalocele 1.04% (3/288 anomalies), in cases MDB22, MDB100, MDB155
Lobulated, fused and horseshoe kidney 1.04% (3/288 anomalies), in cases MDB101, MDB157, MDB399
Anencephaly facies 1.04% (3/288 anomalies), in cases MDB175, MDB381, MDB454
Metatarsus adductus 0.69% (2/288 anomalies), in cases MDB120, MDB179
Cleft palate with cleft lip, unilateral, complete 0.69% (2/288 anomalies), in cases MDB15, MDB221
Persistent left superior vena cava 0.69% (2/288 anomalies), in cases MDB22, MDB105
Aberrant right subclavian artery 0.69% (2/288 anomalies), in cases MDB22, MDB155
Myelomeningocele, lumbosacral 0.69% (2/288 anomalies), in cases MDB88, MDB194
Hydrocephalus 0.69% (2/288 anomalies), in cases MDB100, MDB322
Intestinal malrotation 0.69% (2/288 anomalies), in cases MDB100, MDB399
Renal focal cystic dilatation of collecting tubules 0.69% (2/288 anomalies), in cases MDB100, MDB194
Syndactyly of the feet , simple (webbed), unilateral 0.69% (2/288 anomalies), in cases MDB101, MDB322
Gracile ribs 0.69% (2/288 anomalies), in cases MDB105, MDB322
Aortic valve stenosis, congenital 0.69% (2/288 anomalies), in cases MDB105, MDB201
Hypoplasia of ascending aorta 0.69% (2/288 anomalies), in cases MDB105, MDB201
Right bilobate lung 0.69% (2/288 anomalies), in cases MDB105, MDB518
Scoliosis, congenital 0.69% (2/288 anomalies), in cases MDB105, MDB238
Rocker-bottom feet 0.69% (2/288 anomalies), in cases MDB105, MDB194
Right atrium Enlargement 0.69% (2/288 anomalies), in cases MDB105, MDB201
Flexion contracture of the fingers 0.69% (2/288 anomalies), in cases MDB148, MDB322
Gothic palate 0.69% (2/288 anomalies), in cases MDB155, MDB322
Badly-hemmed ears 0.69% (2/288 anomalies), in cases MDB155, MDB175
Holoanencephaly 0.69% (2/288 anomalies), in cases MDB175, MDB381
Short neck 0.69% (2/288 anomalies), in cases MDB175, MDB322
Small round skull 0.69% (2/288 anomalies), in cases MDB201, MDB322
Camptodactyly, bilateral 0.69% (2/288 anomalies), in cases MDB201, MDB322
Prominent and pointed nose 0.69% (2/288 anomalies), in cases MDB201, MDB201
Syndactyly, simple (webbed), fingers 0.69% (2/288 anomalies), in cases MDB238, MDB224
Axillary pterygia, bilateral 0.69% (2/288 anomalies), in cases MDB238, MDB381
Long philtrum 0.69% (2/288 anomalies), in cases MDB322, MDB518
Polydactyly of the hand, preaxial 0.69% (2/288 anomalies), in cases MDB322, MDB322
Anencephaly 0.69% (2/288 anomalies), in cases MDB381, MDB454
Cleft palate, median posterior 0.69% (2/288 anomalies), in cases MDB381, MDB518
Toe hypoplasia, first, bilateral 0.69% (2/288 anomalies), in cases MDB489, MDB161
Pes cavus 0.35% (1/288 anomalies), in case MDB120
Microtia 0.35% (1/288 anomalies), in case MDB15
Renal agenesis, unilateral 0.35% (1/288 anomalies), in case MDB15
Cerebellar hypoplasia 0.35% (1/288 anomalies), in case MDB15
Cerebral ventriculomegaly 0.35% (1/288 anomalies), in case MDB15
Absence of innominate (brachiocephalic) vein 0.35% (1/288 anomalies), in case MDB22
Trilobate lung, bilateral 0.35% (1/288 anomalies), in case MDB91
Macrocephaly 0.35% (1/288 anomalies), in case MDB100
Flattened nose 0.35% (1/288 anomalies), in case MDB100
Diaphragmatic hernia, congenital 0.35% (1/288 anomalies), in case MDB100
Syndactyly of the feet , simple (webbed), bilateral 0.35% (1/288 anomalies), in case MDB101
Aortic valve atresia 0.35% (1/288 anomalies), in case MDB101
Turned-up nose 0.35% (1/288 anomalies), in case MDB101
Cubital pterygium, bilateral 0.35% (1/288 anomalies), in case MDB105
Axillary pterygia,unilateral 0.35% (1/288 anomalies), in case MDB105
Right ventricular hypoplasia 0.35% (1/288 anomalies), in case MDB105
Aortic isthmus stenosis 0.35% (1/288 anomalies), in case MDB105
Pulmonary artery dilatation, fetal 0.35% (1/288 anomalies), in case MDB105
Platyspondyly 0.35% (1/288 anomalies), in case MDB105
snub-nosed 0.35% (1/288 anomalies), in case MDB105
Polyhydramnios 0.35% (1/288 anomalies), in case MDB105
dextro-Transposition of the great arteries 0.35% (1/288 anomalies), in case MDB105
Cleft palate, bilateral, complete 0.35% (1/288 anomalies), in case MDB105
Dislocation of the knee, congenital, unilateral 0.35% (1/288 anomalies), in case MDB143
Dysplasia of hip, unilateral, congenital 0.35% (1/288 anomalies), in case MDB143
Clindodactyly of 5th finger, bilateral 0.35% (1/288 anomalies), in case MDB148
hypoplasia of the rib 0.35% (1/288 anomalies), in case MDB148
Abnormal formation of the cerebellar gyri 0.35% (1/288 anomalies), in case MDB155
Polydactyly,of the hand, postaxial 0.35% (1/288 anomalies), in case MDB155
Purkinje cell ectopia in the cerebellum 0.35% (1/288 anomalies), in case MDB155
Olfactory nerve, absence of, unilateral 0.35% (1/288 anomalies), in case MDB155
Olfactory nerve hypoplasia,unilateral 0.35% (1/288 anomalies), in case MDB155
Microstomia 0.35% (1/288 anomalies), in case MDB157
Rachischisis, cervical 0.35% (1/288 anomalies), in case MDB175
Exophthalmos, bilateral 0.35% (1/288 anomalies), in case MDB175
Large nose, fetal 0.35% (1/288 anomalies), in case MDB175
Macroglossia 0.35% (1/288 anomalies), in case MDB175
Ureteral duplication, complete, unilateral 0.35% (1/288 anomalies), in case MDB175
Toe hypoplasia, first, unilateral 0.35% (1/288 anomalies), in case MDB179
Absence of six tarsal bones, unilateral 0.35% (1/288 anomalies), in case MDB179
Proximal Focal Femoral Deficiency 0.35% (1/288 anomalies), in case MDB179
Fibular Hemimelia: 0.35% (1/288 anomalies), in case MDB179
Imperforate Anus 0.35% (1/288 anomalies), in case MDB179
Hydronephrosis, congenital, unilateral 0.35% (1/288 anomalies), in case MDB179
Hydroureter, unilateral 0.35% (1/288 anomalies), in case MDB179
Hypospadias, penile 0.35% (1/288 anomalies), in case MDB179
Placenta circumvallata 0.35% (1/288 anomalies), in case MDB179
Marginal subchorionic hematoma 0.35% (1/288 anomalies), in case MDB179
Nephromegaly, bilateral 0.35% (1/288 anomalies), in case MDB194
Double Outlet Right Ventricle, Without Transposition and VSD 0.35% (1/288 anomalies), in case MDB201
Transverse aortic hypoplasia 0.35% (1/288 anomalies), in case MDB201
Right ventricle dilatation 0.35% (1/288 anomalies), in case MDB201
Defective developement of left ventricle 0.35% (1/288 anomalies), in case MDB201
Atrioventricular - channel 0.35% (1/288 anomalies), in case MDB201
Patent Foramen Ovale 0.35% (1/288 anomalies), in case MDB201
Cerebral cyst 0.35% (1/288 anomalies), in case MDB201
Cleft palate, bilateral 0.35% (1/288 anomalies), in case MDB238
Arthrogryposis 0.35% (1/288 anomalies), in case MDB238
Renal hypertropy, fetal, bilateral 0.35% (1/288 anomalies), in case MDB238
Dorsiflexion of foot, unilateral 0.35% (1/288 anomalies), in case MDB224
Talipes equinovarus,unilateral 0.35% (1/288 anomalies), in case MDB224
Hand edema 0.35% (1/288 anomalies), in case MDB224
Constriction Ring Deformity of the upper limbs 0.35% (1/288 anomalies), in case MDB224
Fingers amputation 0.35% (1/288 anomalies), in case MDB224
Cubital deviation of the hand, unilateral 0.35% (1/288 anomalies), in case MDB224
Neck edema 0.35% (1/288 anomalies), in case MDB322
Lower limb hyperextension, Fetal 0.35% (1/288 anomalies), in case MDB322
Polysplenia 0.35% (1/288 anomalies), in case MDB322
Wide space between 1st and 2nd toes, unilateral 0.35% (1/288 anomalies), in case MDB322
Scoliosis, dextroconvex, thoracic 0.35% (1/288 anomalies), in case MDB322
Neuronal migration anomaly 0.35% (1/288 anomalies), in case MDB322
Cortical dysgenesis (CD), diffuse 0.35% (1/288 anomalies), in case MDB322
Absence of neuron differentiation in the basal nuclei. 0.35% (1/288 anomalies), in case MDB322
Arachnodactyly 0.35% (1/288 anomalies), in case MDB381
Large thorax 0.35% (1/288 anomalies), in case MDB381
Prominent shoulder 0.35% (1/288 anomalies), in case MDB381
Narrow pelvis 0.35% (1/288 anomalies), in case MDB381
Flat abdomen 0.35% (1/288 anomalies), in case MDB381
Absence of skull bones 0.35% (1/288 anomalies), in case MDB454
Hydronephrosis, congenital, bilateral 0.35% (1/288 anomalies), in case MDB489
Renal pelvis dilatation, bilateral 0.35% (1/288 anomalies), in case MDB489
Ureterovesical junction stenosis 0.35% (1/288 anomalies), in case MDB489
Lumbosacral agenesis 0.35% (1/288 anomalies), in case MDB518
Relative Macrocephaly 0.35% (1/288 anomalies), in case MDB518
Narrow thorax 0.35% (1/288 anomalies), in case MDB518
Renal agenesis, bilateral 0.35% (1/288 anomalies), in case MDB518
Agenesia of internal genital organs 0.35% (1/288 anomalies), in case MDB518
Thymic hypoplasia 0.35% (1/288 anomalies), in case MDB518
Persistent truncus arteriosus 0.35% (1/288 anomalies), in case MDB518
Right aortic arch 0.35% (1/288 anomalies), in case MDB518
Unilobate lung, unilateral 0.35% (1/288 anomalies), in case MDB518
Gastroschisis 0.35% (1/288 anomalies), in case MDB518
Rachischisis 0.35% (1/288 anomalies), in case MDB518
Vertebral hypoplasia, dorsolumbar 0.35% (1/288 anomalies), in case MDB518
Rib deformation with abnormal numbers, bilateral 0.35% (1/288 anomalies), in case MDB518
Underdeveloped pelvic bones 0.35% (1/288 anomalies), in case MDB518
Giant omphalocele 0.35% (1/288 anomalies), in case MDB158
Olfactory nerve, absence of, bilateral 0.35% (1/288 anomalies), in case MDB161
Trigonocephaly 0.35% (1/288 anomalies), in case MDB161
Thalamic nuclei centrum medianum fusion 0.35% (1/288 anomalies), in case MDB161
Olfactory bulbs, absence of 0.35% (1/288 anomalies), in case MDB161
Holoprosencephaly 0.35% (1/288 anomalies), in case MDB161

Terminology and coding

References

No reference related to Overlapping fingers is available at the moment.

Last modified: 2008-12-04 16:11:00 by farideh

Created: 2008-02-14 00:00:00 by phsaw

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