Glaucoma, primary closed-angle

Preferred Label : Glaucoma, primary closed-angle;

Symbol : GLCC;

CISMeF acronym : GLCC;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the type XVIII collagen, alpha-1 polypeptide gene (COL18A1, 120328.0010);

Prefixed ID : #618880;

Details

Origin ID

618880;

UMLS CUI

C5394374;

Genes related to phenotype
- Collagen, type XVIII, alpha-1 [OMIM gene]
HPO term(s)
- Angle closure glaucoma [HPO term]
- Anterior synechiae of the anterior chamber [HPO term]
- Autosomal dominant inheritance [HPO term]
- Increased cup-to-disc ratio [HPO term]
- Ocular hypertension [HPO term]
- Visual field defect [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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