Link to this page
Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/608068
http://purl.bioontology.org/ontology/OMIM/608068
|
|---|---|
| Preferred Name | NEUTROPHILIC DERMATOSIS, ACUTE FEBRILE |
| Synonyms |
SWEET SYNDROME
GOMM-BUTTON DISEASE
SS
PYRIN-ASSOCIATED AUTOINFLAMMATORY DISEASE
AFND
PAAND
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
SWEET SYNDROME
GOMM-BUTTON DISEASE
SS
PYRIN-ASSOCIATED AUTOINFLAMMATORY DISEASE
AFND
PAAND
See more
See less
|
|---|---|
| prefLabel | NEUTROPHILIC DERMATOSIS, ACUTE FEBRILE
|
| Gene Symbol |
PAAND
FMF
MEFV
MEF
|
| Scope Statement | Caused by mutation in the MEFV innate immunity regulator, pyrin gene (MEFV, 608107.0021) [MOLECULAR BASIS]
Incomplete penetrance [MISCELLANEOUS]
Variable expressivity [MISCELLANEOUS]
Onset in childhood [MISCELLANEOUS]
|
| type | |
| Has manifestation |
See more
See less
|
| tui | T047
|
| Gene Locus | 16p13
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 608068
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C0085077
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |