Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Synbrakydaktyli i hånd |
Is a |
False |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
Brachydactyly-all 3 phalanges |
Is a |
True |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
Brachydactyly-missing phalanx |
Is a |
True |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
Brakydaktyli af fingre, uspecificeret |
Is a |
False |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
Brachysyndactyly of thumb |
Is a |
False |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
Symbrachydactyly |
Is a |
False |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
Craniosynostosis with facial dysmorphism and brachydactyly syndrome |
Is a |
False |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
A rare, genetic, epilepsy syndrome characterized by epilepsy, palpebral conjunctival telangiectasias, borderline to moderate intellectual disability, diminished serum IgA levels, shortened fifth fingers and dysmorphic facial features (including frontal hirsutism, synophrys, anteverted nostrils, prominent ears, long philtrum, irregular teeth implantation, micrognathia). No new cases have been described in the literature since 1978. |
Is a |
True |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|
Symbrachydactyly of digit of hand (disorder) |
Is a |
True |
Brachydactyly of hand (disorder) |
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. |
Is a |
True |
Brachydactyly of hand (disorder) |
Inferred relationship |
Some |
|