Lymphedema and cerebral arteriovenous anomaly

Preferred Label : Lymphedema and cerebral arteriovenous anomaly;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 152900;

Details

Origin ID

152900;

UMLS CUI

C1835272;

Currated CISMeF NLP mapping
- Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome [ORDO Disease]
- lymphedema and cerebral arteriovenous anomaly [MeSH concept]
- lymphedema and cerebral arteriovenous anomaly [MeSH Supplementary Concept]
HPO term(s)
- Abnormal cerebral vascular morphology [HPO term]
- Autosomal dominant inheritance [HPO term]
- Lymphedema [HPO term]
- Pulmonary arterial hypertension [HPO term]
ORDO concept(s)
- Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome [ORDO Disease]
- lymphedema and cerebral arteriovenous anomaly [MeSH Supplementary Concept]
- lymphedema and cerebral arteriovenous anomaly [MeSH concept]

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