FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hypotrichosis 7 ID (Ontology) DOID:0110704 (Human Disease)
Definition A hypotrichosis that has_material_basis_in a autosomal recessive mutation of the LIPH gene on chromosome 3q27.2.
Also Known As "hypotrichosis, localized, autosomal recessive 2" ; "HYPT7" ; "LAH2" (for all, see Synonyms field below)
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 Genes
 hypotrichosis 7      22
 for disease ribbon | hypotrichosis 7      22
 model of | hypotrichosis 7      22
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
hair disease                     |
 |__hypotrichosis________________|
                                 hypotrichosis 7  22 rec.
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Is a autosomal recessive disease
hypotrichosis
Part of
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Synonyms
  • "hypotrichosis, localized, autosomal recessive 2" EXACT
    "HYPT7" EXACT OMO:0003012
    "LAH2" EXACT OMO:0003012
    "total hyptrichosis, Mari type" EXACT
Secondary IDs
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MIM:604379