hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration

Preferred Label : hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0564903;

UMLS CUI

C1846582;

Automatic exact mappings (from CISMeF team)
- HARP syndrome [ICD-11 More detail]
Currated CISMeF NLP mapping
- HARP syndrome [ORDO Disease]
- Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration [OMIM Phenotype]
Related record
- hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- HARP syndrome [ORDO Disease]
- Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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