Preferred Name |
Vohwinkel syndrome |
|
Synonyms |
VS |
|
Definitions |
(VS) - VS is an autosomal dominant disease characterized by hyperkeratosis, constriction on fingers and toes and congenital deafness. |
|
ID |
http://identifiers.org/omim/124500 |
|
altLabel |
VS |
|
definition |
(VS) - VS is an autosomal dominant disease characterized by hyperkeratosis, constriction on fingers and toes and congenital deafness. |
|
id |
OMIM:124500 |
|
notation |
OMIM:124500 |
|
prefLabel |
Vohwinkel syndrome |
|
subClassOf |
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