Preferred Name |
Vohwinkel syndrome |
|
Synonyms |
|
|
Definitions |
(VS): VS is an autosomal dominant disease characterized by hyperkeratosis, constriction on fingers and toes and congenital deafness. |
|
ID |
http://purl.obolibrary.org/obo/OMIM_124500 |
|
definition |
(VS): VS is an autosomal dominant disease characterized by hyperkeratosis, constriction on fingers and toes and congenital deafness. |
|
has_obo_namespace |
cell_cycle_ontology |
|
id |
OMIM:124500 |
|
label |
Vohwinkel syndrome |
|
notation |
OMIM:124500 |
|
prefLabel |
Vohwinkel syndrome |
|
treeView | ||
subClassOf |
Create mapping