symbol withdrawn CILD2

Preferred Label : symbol withdrawn CILD2;

Obsolete resource : true;

Approved symbol HGNC : CILD2;

Alias symbols HGNC : PCD;

Chromosome HGNC : 19q13.3-qter;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:1979;

Automatic exact mappings (from CISMeF team)
- Ciliary dyskinesia, primary, 2 [OMIM Phenotype]
- Premature centromere division [OMIM Phenotype]
Replaced by
- dynein axonemal assembly factor 3 [HGNC gene]

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