Pupillary membrane, persistence of

Preferred Label : Pupillary membrane, persistence of;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant; ? same as Rieger syndrome;

Prefixed ID : 178900;

Details

Origin ID

178900;

UMLS CUI

C0271130;

Currated CISMeF NLP mapping
- Persistence of the pupillary membrane [PASCAL descriptor]
- Persistent Pupillary Membrane [NCIt concept]
- Persistent pupillary membrane [HPO term]
- Persistent pupillary membrane [MedDRA Preferred Term]
- Persistent pupillary membranes [ICD-11 Category]
- Persistent pupillary membranes (disorder) [SNOMED CT concept]
- persistent pupillary membranes [SNOMED Notion]
- pupillary membrane, persistence of [MeSH concept]
- pupillary membrane, persistence of [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Developmental cataract [HPO term]
- Increased corneal diameter [HPO term]
- Megalocornea [HPO term]
- Persistent pupillary membrane [HPO term]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- pupillary membrane, persistence of [MeSH Supplementary Concept]
- pupillary membrane, persistence of [MeSH concept]

Keyword's position in hierarchy(ies) :

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