Ichthyosis Vulgaris
Disease ID: disease_node_8589
Connections displayed (default: 10).
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| Dbxref | GARD:6752, ICD10CM:Q80.0, MESH:D016112, MIM:146700, NCI:C84778, SNOMEDCT_US_2023_03_01:205551004, UMLS_CUI:C0079584 |
|---|---|
| Subclassof | DOID_0050736, DOID_1697 |
| Data Source | DOID, MESH |
| Synonyms | Dominant congenital ichthyosiform erythroderma |
| Mesh Id | D016112 |
| Mesh Label | Ichthyosis Vulgaris |
| Mesh Subclassof | D012873, D007057 |
| Doid Label | ichthyosis vulgaris |
| Doid Description | An ichthyosis that has_material_basis_in heterozygous mutation in the filaggrin gene (FLG) on chromosome 1q21 and is characterized by dead skin cells accumulate in thick, dry scales on your skin's surface. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_8589 |
| Doid Id | DOID_1702 |
| Label | Ichthyosis Vulgaris |
- Outgoing r'ship
SUBCLASS_OFto/from Ichthyosis(ID:disease_node_4236) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)