Restrictive dermopathy 2

Preferred Label : Restrictive dermopathy 2;

Symbol : RSDM2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Restrictive dermopathy 2, lethal;

Prefixed ID : #619793;

Details

Origin ID

619793;

UMLS CUI

C5676942;

Genes related to phenotype
- Lamin a/C [OMIM gene]
ORDO concept(s)
- Restrictive dermopathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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