Ciliary dyskinesia, primary, 48, without situs inversus

Preferred Label : Ciliary dyskinesia, primary, 48, without situs inversus;

Symbol : CILD48;

Type : Phenotype, molecular basis known;

Prefixed ID : #620032;

Details

Origin ID

620032;

UMLS CUI

C5774214;

Genes related to phenotype
- Nme/nm23 family, member 5 [OMIM gene]
ORDO concept(s)
- Primary ciliary dyskinesia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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