FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term monilethrix ID (Ontology) DOID:0050472 (Human Disease)
Definition A hair disease that is characterized by short, easily broken hair that results in alopecia and has_material_basis_in mutations in genes for type II hair cortex keratins.
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autosomal genetic disease
 |__autosomal dominant disease__
integumentary system disease    |
 |__hair disease________________|
                                monilethrix
                                 |__monilethrix 1
                                 |__monilethrix 2
                                 |__monilethrix 3
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Is a autosomal dominant disease
hair disease
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Synonyms
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GARD:93
ICD10CM:Q84.1
MESH:D056734
NCI:C84894
SNOMEDCT_US_2023_03_01:69488000
UMLS_CUI:C0546966