Hydrocephalus, endocardial fibroelastosis, and cataracts

Preferred Label : Hydrocephalus, endocardial fibroelastosis, and cataracts;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Hec syndrome;

Inheritance : Genetic vs. viral;

Prefixed ID : 600559;

Details

Origin ID

600559;

UMLS CUI

C1833607;

Currated CISMeF NLP mapping
- HEC syndrome [ORDO Disease]
- Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) [SNOMED CT concept]
- Hydrocephalus, endocardial fibroelastosis, and cataracts [MeSH concept]
- hydrocephalus, endocardial fibroelastosis, and cataracts [MeSH Supplementary Concept]
HPO term(s)
- Communicating hydrocephalus [HPO term]
- Death in infancy [HPO term]
- Developmental cataract [HPO term]
- Endocardial fibroelastosis [HPO term]
- Polyhydramnios [HPO term]
ORDO concept(s)
- HEC syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- HEC syndrome [ORDO Disease]
- Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) [SNOMED CT concept]
- Hydrocephalus, endocardial fibroelastosis, and cataracts [MeSH concept]
- hydrocephalus, endocardial fibroelastosis, and cataracts [MeSH Supplementary Concept]

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