FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term adermatoglyphia ID (Ontology) DOID:0111357 (Human Disease)
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.
Also Known As "Absence of fingerprints" ; "ADERM" ; "ADG" (for all, see Synonyms field below)
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DO.org
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 Genes
 adermatoglyphia       1
 for disease ribbon | adermatoglyphia       1
 model of | adermatoglyphia       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
integumentary system disease    |
 |__skin disease________________|
                                adermatoglyphia  1 rec.
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Is a autosomal dominant disease
skin disease
Part of
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Synonyms
  • "Absence of fingerprints" EXACT
    "ADERM" EXACT OMO:0003012
    "ADG" EXACT OMO:0003012
    "Congenital absence of fingerprints" EXACT
    "Immigration delay disease" EXACT
    "Isolated congenital adermatoglyphia" EXACT
Secondary IDs
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GARD:12550
MIM:136000
ORDO:289465