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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/604117
http://purl.bioontology.org/ontology/OMIM/604117
|
|---|---|
| Preferred Name | VOHWINKEL SYNDROME, VARIANT FORM |
| Synonyms |
LORICRIN KERATODERMA
VOHWINKEL SYNDROME WITH ICHTHYOSIS
MUTILATING KERATODERMA WITH ICHTHYOSIS
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
LORICRIN KERATODERMA
VOHWINKEL SYNDROME WITH ICHTHYOSIS
MUTILATING KERATODERMA WITH ICHTHYOSIS
|
|---|---|
| prefLabel | VOHWINKEL SYNDROME, VARIANT FORM
|
| Gene Symbol |
LOR
LORICRIN
|
| Scope Statement | Caused by mutation in the loricrin cornified envelope precursor protein gene (LORICRIN, 152445.0001) [MOLECULAR BASIS]
|
| type | |
| Has manifestation |
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|
| tui | T047
|
| Gene Locus | 1q21
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 604117
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C1858805
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |