Search Ontology:
Human Disease
adermatoglyphia
- Term ID
- DOID:0111357
- Synonyms
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- Absence of fingerprints
- ADERM
- ADG
- Congenital absence of fingerprints
- Immigration delay disease
- Isolated congenital 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
- References
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- GARD:12550
- MIM:136000
- ORDO:289465
- Ontology
- Human Disease ( DOID:0111357 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models