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loading...| Preferred Name |
Vohwinkel syndrome |
|
| Synonyms |
Mutilating keratoderma |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C536457 |
|
| altLabel |
Mutilating keratoderma Palmoplantar Keratoderma Mutilans Vohwinkel Congenital Deafness with Keratopachydermia and Constrictions of Fingers and Toes Keratoderma hereditarium mutilans Ppk Mutilans Vohwinkel Palmoplantar Keratoderma Mutilans |
|
| cui |
C0265964 |
|
| HM |
D006319 D000015 D006228 D007645 |
|
| Inverse of RB |
0 |
|
| Mapped to |
http://purl.bioontology.org/ontology/MESH/D006319 http://purl.bioontology.org/ontology/MESH/D000015 |
|
| MDA |
20100825 |
|
| MeSH Frequency |
15 |
|
| MMR |
20131024 |
|
| notation |
C536457 |
|
| prefLabel |
Vohwinkel syndrome |
|
| SC |
3 |
|
| Scope Statement |
Deafness, congenital, with keratopachydermia and constrictions of fingers and toes |
|
| TERMUI |
T739405 T842667 T842668 T842670 T842669 T739402 T739404 |
|
| TH |
OMIM (2013) GHR (2014) ORD (2010) |
|
| tui |
T019 |
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