Cataract 35 - CISMeF

Preferred Label : Cataract 35;

Symbol : CTRCT35;

CISMeF acronym : CATCN1; CTRCT35;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Cataract, congenital nuclear, autosomal recessive 1; CATCN1;

Inheritance : Autosomal recessive;

Prefixed ID : %609376;

Details

Origin ID

609376;

UMLS CUI

C1836272;

Currated CISMeF NLP mapping
- cataract 35 [DO Concept]
- cataract, congenital nuclear, autosomal recessive 1 [MeSH concept]
- cataract, congenital nuclear, autosomal recessive 1 [MeSH Supplementary Concept]
DO Cross reference
- cataract 35 [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Cataract [HPO term]
ORDO concept(s)
- Early-onset non-syndromic cataract [ORDO Disease]
- Early-onset nuclear cataract [ORDO Disease]
- Early-onset partial cataract [ORDO Disease]
- Early-onset zonular cataract [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cataract 35 [DO Concept]
- cataract, congenital nuclear, autosomal recessive 1 [MeSH Supplementary Concept]
- cataract, congenital nuclear, autosomal recessive 1 [MeSH concept]

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