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| Term | hypotrichosis | ID (Ontology) | DOID:4535 (Human Disease) |
| Definition | A hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has_material_basis_in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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integumentary system disease |__hair disease |__hypotrichosis 27 rec. |__alopecia 1 rec. | |__alopecia universalis 1 rec. | |__androgenic alopecia | |__atrichia with papular lesions 1 rec. | |__loose anagen hair syndrome | |__telogen effluvium |__congenital hypotrichosis with juvenile macular dystrophy |__hypotrichosis 1 |__hypotrichosis 2 |__hypotrichosis 3 |__hypotrichosis 4 |__hypotrichosis 5 2 rec. |__hypotrichosis 6 |__hypotrichosis 7 22 rec. |__hypotrichosis 8 |__hypotrichosis 9 |__hypotrichosis 10 |__hypotrichosis 11 1 rec. |__hypotrichosis 12 1 rec. |__hypotrichosis 13 |__hypotrichosis 14 |__hypotrichosis 15 |__hypotrichosis of eyelid |
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| Is a | hair disease | ||
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External Crossreferences & Linkouts
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MESH:D007039 MIM:PS605389 ORDO:55654 SNOMEDCT_US_2023_03_01:53602002 UMLS_CUI:C0020678 |
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