Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire thumb |
Is a |
True |
Entire digit of hand |
Inferred relationship |
Some |
|
Entire finger |
Is a |
True |
Entire digit of hand |
Inferred relationship |
Some |
|
Phalanx of supernumerary digit of hand |
partie de |
False |
Entire digit of hand |
Additional relationship |
Some |
|
Entire interphalangeal joint of hand |
partie de |
False |
Entire digit of hand |
Additional relationship |
Some |
|
Interphalangeal joint of hand structure (body structure) |
partie de |
False |
Entire digit of hand |
Additional relationship |
Some |
|
Structure of nail bed of digit of hand (body structure) |
partie de |
False |
Entire digit of hand |
Additional relationship |
Some |
|
Brachydactyly-all 3 phalanges |
Finding site |
True |
Entire digit of hand |
Inferred relationship |
Some |
1 |
Brachydactyly-missing phalanx |
Finding site |
True |
Entire digit of hand |
Inferred relationship |
Some |
1 |
Brachydactyly of hand |
Finding site |
True |
Entire digit of hand |
Inferred relationship |
Some |
1 |
Synbrachydactyly of hand |
Finding site |
False |
Entire digit of hand |
Inferred relationship |
Some |
1 |
A rare genetic syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy characterized by duplication anomalies such as triphalangeal thumbs, phalangeal duplication of other digits, and polydactyly, associated with highly variable combinations of ectrodactyly, brachydactyly, and syndactyly of hands and/or feet. Severe nail dysplasia or absence of nails is also observed. |
Finding site |
False |
Entire digit of hand |
Inferred relationship |
Some |
2 |
Craniosynostosis with facial dysmorphism and brachydactyly syndrome |
Finding site |
False |
Entire digit of hand |
Inferred relationship |
Some |
4 |
Heart-hand syndrome type 3 is a very rare heart-hand syndrome, described in three members of a Spanish family to date, which is characterized by a cardiac conduction defect (sick sinus, bundle-branch block) and brachydactyly, resembling brachydactyly type C of the hands, affecting principally the middle phalanges in conjunction with an extra ossicle on the proximal phalanx of both index fingers. Feet abnormalities are more subtle. |
Finding site |
False |
Entire digit of hand |
Inferred relationship |
Some |
4 |
Guttmacher syndrome is an extremely rare syndrome characterized by hypoplastic thumbs and halluces, 5th finger clinobrachydactyly, postaxial polydactyly of the hands, short or uniphalangeal 2nd toes with absent nails and hypospadias. |
Finding site |
False |
Entire digit of hand |
Inferred relationship |
Some |
7 |
Symbrachydactyly of digit of hand (disorder) |
Finding site |
True |
Entire digit of hand |
Inferred relationship |
Some |
2 |
A rare genetic syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy characterized by duplication anomalies such as triphalangeal thumbs, phalangeal duplication of other digits, and polydactyly, associated with highly variable combinations of ectrodactyly, brachydactyly, and syndactyly of hands and/or feet. Severe nail dysplasia or absence of nails is also observed. |
Finding site |
True |
Entire digit of hand |
Inferred relationship |
Some |
1 |
Craniosynostosis with facial dysmorphism and brachydactyly syndrome |
Finding site |
False |
Entire digit of hand |
Inferred relationship |
Some |
3 |
Heart-hand syndrome type 3 is a very rare heart-hand syndrome, described in three members of a Spanish family to date, which is characterized by a cardiac conduction defect (sick sinus, bundle-branch block) and brachydactyly, resembling brachydactyly type C of the hands, affecting principally the middle phalanges in conjunction with an extra ossicle on the proximal phalanx of both index fingers. Feet abnormalities are more subtle. |
Finding site |
True |
Entire digit of hand |
Inferred relationship |
Some |
2 |
Guttmacher syndrome is an extremely rare syndrome characterized by hypoplastic thumbs and halluces, 5th finger clinobrachydactyly, postaxial polydactyly of the hands, short or uniphalangeal 2nd toes with absent nails and hypospadias. |
Finding site |
True |
Entire digit of hand |
Inferred relationship |
Some |
3 |
Entire digit of right hand (body structure) |
Is a |
True |
Entire digit of hand |
Inferred relationship |
Some |
|
Entire digit of left hand |
Is a |
True |
Entire digit of hand |
Inferred relationship |
Some |
|
A rare genetic, multiple congenital anomalies syndrome characterized by short stature, hand brachydactyly with hypoplastic distal phalanges, global development delay, intellectual disability, and more variably seizures, obesity, and craniofacial dysmorphism that includes microcephaly, high forehead, flat face, hypertelorism, deep set eyes, flat nasal bridge, averted nostrils, long philtrum, thin lip vermilion, and short neck. |
Finding site |
True |
Entire digit of hand |
Inferred relationship |
Some |
1 |
A rare dysostosis with brachydactyly characterised by short digits predominantly on the preaxial (radial) side resulting in stub thumbs, short index fingers and a cutaneous web between the first and second fingers. No extraskeletal manifestations are present. |
Finding site |
True |
Entire digit of hand |
Inferred relationship |
Some |
1 |