Cataract, nonnuclear polymorphic congenital, autosomal dominant

Preferred Label : Cataract, nonnuclear polymorphic congenital, autosomal dominant;

Obsolete resource : true;

Moved to : 115700;

Alternative titles and symbols : Ccp; Pcc; Cataract, polymorphic congenital;

Inheritance : Autosomal dominant;

Prefixed ID : 601286;

Details

Origin ID

601286;

UMLS CUI

C1832526;

Automatic exact mappings (from CISMeF team)
- Adrenal Gland Pheochromocytoma [NCIt concept]
- Cataract congenital dominant non nuclear [MeSH concept]
- Cyclic Citrullinated Peptide Antibody [NCIt concept]
Currated CISMeF NLP mapping
- cataract congenital dominant non nuclear [MeSH Supplementary Concept]
False automatic mappings
- 1-piperidinocyclohexanecarbonitrile (substance) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Cataract congenital dominant non nuclear [MeSH concept]
- cataract congenital dominant non nuclear [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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