Lipodystrophy, congenital generalized - CISMeF

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CISMeF

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Lipodystrophy, congenital generalizedOMIM phenotypic series

Preferred Label : Lipodystrophy, congenital generalized;

Details

Origin ID

PS608594;

Currated CISMeF NLP mapping
- Berardinelli-Seip Congenital Lipodystrophy [NCIt concept]
- Congenital generalised lipodystrophy [ICD-11 Sub-sub category]
- Congenital generalised lipodystrophy [MedDRA Preferred Term]
- Congenital generalized lipodystrophy [HPO term]
- Congenital generalized lipodystrophy [MedDRA LLT]
- Congenital generalized lipodystrophy [ORDO Disease]
- Congenital total lipodystrophy (disorder) [SNOMED CT concept]
- congenital generalized lipodystrophy [DO Concept]
- congenital generalized lipodystrophy [Disease (Nov.)]
- familial generalized lipodystrophy [SNOMED Notion]
- lipodystrophy, congenital generalized [MeSH Descriptor]
- lipodystrophy, congenital generalized [MeSH concept]
DO Cross reference
- congenital generalized lipodystrophy [DO Concept]

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02/05/2025

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