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| General Information | |||
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| Term | Mulvihill-Smith syndrome | ID (Ontology) | DOID:0061154 (Human Disease) |
| Definition | A progeroid syndrome that is characterized by premature aging, multiple pigmented nevi, lack of facial subcutaneous fat, microcephaly, short stature, sensorineural hearing loss, and impaired intellectual development. | ||
| Also Known As | "progeroid short stature with pigmented nevi" | ||
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| DO.org | |||
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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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syndrome |__progeroid syndrome |__Mulvihill-Smith syndrome |
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| Is a | progeroid syndrome | ||
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External Crossreferences & Linkouts
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MIM:176690 ORDO:2959 |
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