cataract, juvenile, with microcornea and glucosuria

Preferred Label : cataract, juvenile, with microcornea and glucosuria;

MeSH note : mutation on Monocarboxylate transporter 12;

Origin ID

C567434;

UMLS CUI

C2677587;

Currated CISMeF NLP mapping
- Cataract 47 [OMIM Phenotype]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
- glycosuria, renal [MeSH Descriptor]
Record concept(s)
- cataract, juvenile, with microcornea and glucosuria [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Juvenile cataract-microcornea-renal glucosuria syndrome [ORDO Disease]