Adermatoglyphia
Disease ID: disease_node_20038
Connections displayed (default: 10).
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| Dbxref | GARD:12550, MIM:136000, ORDO:289465 |
|---|---|
| Subclassof | DOID_0050736, DOID_37 |
| Data Source | DOID |
| Synonyms | ADERM, ADG, Absence of fingerprints, Congenital absence of fingerprints, Immigration delay disease, Isolated congenital adermatoglyphia |
| Disease Has Location | UBERON_0002398, UBERON_0002387 |
| Doid Label | adermatoglyphia |
| Doid Description | A skin disease characterized by lack of epidermal ridges on the fingers, toes, palms and soles that has_material_basis_in heterozygous mutation in the SMARCAD1 gene on chromosome 4q22.3. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_20038 |
| Doid Id | DOID_0111357 |
| Label | Adermatoglyphia |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Skin Diseases(ID:disease_node_6968) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Skin Diseases, Genetic(ID:disease_node_6970) (Disease)