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DO Term : adermatoglyphia [DOID:0111357] Disease Ontology

Namespace

disease_ontology

Obsolete

false

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.

synonyms:
Absence of fingerprints,
Isolated congenital adermatoglyphia,
OMIM:136000,
ADG,
Immigration delay disease,
136000,
ORDO:289465,
GARD:12550,
ADERM,
Congenital absence of fingerprints

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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