| Metadata | |
|---|---|
| ID | DOID:0111357 |
| PURL | http://purl.obolibrary.org/obo/DOID_0111357 Copy |
| Name | adermatoglyphia |
| Definition | 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. https://www.ncbi.nlm.nih.gov/pubmed/21820097 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
Absence of fingerprints [EXACT] ADERM [EXACT] ADG [EXACT] Congenital absence of fingerprints [EXACT] Immigration delay disease [EXACT] Isolated congenital adermatoglyphia [EXACT] |
| Parent Relationships |
is_a autosomal dominant disease is_a skin disease |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance disease has basis in some gene |