Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire thumb |
Is a |
True |
Entire digit of hand (body structure) |
Inferred relationship |
Some |
|
Entire finger |
Is a |
True |
Entire digit of hand (body structure) |
Inferred relationship |
Some |
|
Phalanx of supernumerary digit of hand |
del af |
False |
Entire digit of hand (body structure) |
Additional relationship |
Some |
|
Entire interphalangeal joint of hand |
del af |
False |
Entire digit of hand (body structure) |
Additional relationship |
Some |
|
Interphalangeal joint of hand structure (body structure) |
del af |
False |
Entire digit of hand (body structure) |
Additional relationship |
Some |
|
Structure of nail bed of digit of hand (body structure) |
del af |
False |
Entire digit of hand (body structure) |
Additional relationship |
Some |
|
Brachydactyly-all 3 phalanges |
Finding site |
True |
Entire digit of hand (body structure) |
Inferred relationship |
Some |
1 |
Brachydactyly-missing phalanx |
Finding site |
True |
Entire digit of hand (body structure) |
Inferred relationship |
Some |
1 |
Brachydactyly of hand (disorder) |
Finding site |
True |
Entire digit of hand (body structure) |
Inferred relationship |
Some |
1 |
Synbrakydaktyli i hånd |
Finding site |
False |
Entire digit of hand (body structure) |
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 (body structure) |
Inferred relationship |
Some |
2 |
Craniosynostosis with facial dysmorphism and brachydactyly syndrome |
Finding site |
False |
Entire digit of hand (body structure) |
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 (body structure) |
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 (body structure) |
Inferred relationship |
Some |
7 |
Symbrachydactyly of digit of hand (disorder) |
Finding site |
True |
Entire digit of hand (body structure) |
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 (body structure) |
Inferred relationship |
Some |
1 |
Craniosynostosis with facial dysmorphism and brachydactyly syndrome |
Finding site |
False |
Entire digit of hand (body structure) |
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 (body structure) |
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 (body structure) |
Inferred relationship |
Some |
3 |
Entire digit of right hand (body structure) |
Is a |
True |
Entire digit of hand (body structure) |
Inferred relationship |
Some |
|
Entire digit of left hand |
Is a |
True |
Entire digit of hand (body structure) |
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 (body structure) |
Inferred relationship |
Some |
1 |