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| Term | ichthyosis follicularis-alopecia-photophobia syndrome 1 | ID (Ontology) | DOID:0111821 (Human Disease) |
| Definition | A syndrome characterized by ichthyosis follicularis, atrichia, and photophobia that has_material_basis_in hemizygous or homozygous mutation in the MBTPS2 gene on chromosome Xp22.12. | ||
| Also Known As | "ichthyosis follicularis-atrichia-photophobia syndrome 1" ; "IFAP syndrome 1" ; "IFAP syndrome 1 with or without BRESHECK syndrome" | ||
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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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X-linked monogenic disease |__X-linked recessive disease__ disease | |__syndrome____________________| ichthyosis follicularis-alopecia-photophobia syndrome 1 1 rec. |
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X-linked recessive disease syndrome |
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GARD:2952 MESH:C536085 MIM:308205 ORDO:2273 UMLS_CUI:C1839988 |
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