OBO ID: DOID:0111357
Term Name: adermatoglyphia Search Ontology:
Synonyms:
  • 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:
Ontology: Human Disease   ( DOID:0111357 )
OTHER adermatoglyphia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SMARCAD1 Adermatoglyphia 136000
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None