Stomatocytosis ii

Preferred Label : Stomatocytosis ii;

Obsolete resource : true;

Moved to : 194380;

Inheritance : Autosomal dominant;

Prefixed ID : 185010;

Details

Origin ID

185010;

UMLS CUI

C1861454;

Automatic exact mappings (from CISMeF team)
- Stomatocytosis [PASCAL descriptor]
Currated CISMeF NLP mapping
- stomatocytosis II [MeSH concept]
- stomatocytosis II [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- stomatocytosis II [MeSH Supplementary Concept]
- stomatocytosis II [MeSH concept]
Validated automatic mappings to NTBT
- Hereditary stomatocytosis [ORDO Disease]

Keyword's position in hierarchy(ies) :

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