Glaucoma 3, primary infantile, b

Preferred Label : Glaucoma 3, primary infantile, b;

Symbol : GLC3B;

CISMeF acronym : GLC3B;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Glaucoma, primary congenital, type b; Glc3, type b;

Description : For a general phenotypic description and a discussion of primary congenital glaucoma (PCG), see GLC3A (231300).;

Inheritance : Autosomal recessive.;

Prefixed ID : %600975;

Details

Origin ID

600975;

UMLS CUI

C1832977;

Currated CISMeF NLP mapping
- glaucoma 3, primary infantile, B [MeSH concept]
- glaucoma 3, primary infantile, B [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Primary congenital glaucoma [HPO term]
ORDO concept(s)
- Congenital glaucoma [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- glaucoma 3, primary infantile, B [MeSH Supplementary Concept]
- glaucoma 3, primary infantile, B [MeSH concept]

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