Lymphatic malformation 12

Preferred Label : Lymphatic malformation 12;

Symbol : LMPHM12;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Central conducting lymphatic anomaly; CCLA;

Prefixed ID : #620014;

Détails

Origin ID

620014;

UMLS CUI

C5774203;

Genes related to phenotype
- Myod family inhibitor domain-containing protein [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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