Search Ontology:
Human Disease

adermatoglyphia

Term ID
DOID:0111357
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models