Iris pigment epithelium anomalies

Preferred Label : Iris pigment epithelium anomalies;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Cysts of iris pigment epithelium; Ruffles and cysts of iris pigment epithelium;

Inheritance : Autosomal dominant;

Prefixed ID : %601616;

Details

Origin ID

601616;

UMLS CUI

C1866608;

Currated CISMeF NLP mapping
- iris pigment epithelium anomalies [MeSH concept]
- iris pigment epithelium anomalies [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Iris cyst [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- iris pigment epithelium anomalies [MeSH Supplementary Concept]
- iris pigment epithelium anomalies [MeSH concept]

Keyword's position in hierarchy(ies) :

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