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| General Information | |||
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| Term | Ramon syndrome | ID (Ontology) | DOID:0070650 (Human Disease) |
| Definition | A syndrome characterized by cherubism, gingival fibromatosis, epilepsy, mental deficiency, hypertrichosis, and stunted growth. | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal recessive disease__ disease | |__syndrome_____________________| Ramon syndrome |
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Relationships
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| Is a |
autosomal recessive disease syndrome |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:7523 MESH:C535285 MIM:266270 ORDO:3019 UMLS_CUI:C0796133 |
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