Search Ontology:
Human Disease

hypotrichosis 5

Term ID
DOID:0110702
Synonyms
  • HYPT5
  • Marie Unna Hereditary Hypotrichosis 2
  • MUHH2
Definition
A hypotrichosis that has_material_basis_in a mutation on chromosome 1p21.1-q21.3. https://www.ncbi.nlm.nih.gov/pubmed/16185270
References
Ontology
Human Disease   ( DOID:0110702 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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