Lymphatic malformation 10

Preferred Label : Lymphatic malformation 10;

Symbol : LMPHM10;

Type : Phenotype, molecular basis known;

Prefixed ID : #619369;

Origin ID

619369;

UMLS CUI

C5543531;

Genes related to phenotype
- Angiopoietin 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hydrocele testis [HPO term]
- Infantile onset [HPO term]
- Lymphedema [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]