Lymphatic malformation 9 - CISMeF

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CISMeF

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Lymphatic malformation 9OMIM Phenotype

Preferred Label : Lymphatic malformation 9;

Symbol : LMPHM9;

Type : Phenotype, molecular basis known;

Prefixed ID : #619319;

Details

Origin ID

619319;

UMLS CUI

C5543365;

Genes related to phenotype
- Cadherin egf lag seven-pass g-type receptor 1 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Predominantly lower limb lymphedema [HPO term]
- Tortuous lymphatic vessels [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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12/07/2025

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