Pallidal degeneration, progressive, with retinitis pigmentosa

Preferred Label : Pallidal degeneration, progressive, with retinitis pigmentosa;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive vs. X-linked;

Prefixed ID : 260200;

Details

Origin ID

260200;

UMLS CUI

C1850101;

Currated CISMeF NLP mapping
- pallidal degeneration, progressive, with retinitis pigmentosa [MeSH concept]
- pallidal degeneration, progressive, with retinitis pigmentosa [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- pallidal degeneration, progressive, with retinitis pigmentosa [MeSH Supplementary Concept]
- pallidal degeneration, progressive, with retinitis pigmentosa [MeSH concept]

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