Lymphatic malformation 11 - CISMeF

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CISMeF

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Lymphatic malformation 11OMIM Phenotype

Preferred Label : Lymphatic malformation 11;

Symbol : LMPHM11;

Type : Phenotype, molecular basis known;

Prefixed ID : #619401;

Details

Origin ID

619401;

UMLS CUI

C5543614;

Genes related to phenotype
- Tyrosine kinase with immunoglobulin and egf factor homology domains 1 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Juvenile onset [HPO term]
- Lymphedema [HPO term]
- Pedal edema [HPO term]
- Young adult onset [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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02/06/2025

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