Disease #04649 (CILD-32 (dyskinesia, ciliary, primary, type 32 (CILD-32)), OMIM:616481)

Official abbreviation CILD-32
Name dyskinesia, ciliary, primary, type 32 (CILD-32)
OMIM ID 616481
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene RSPH3
Associated tissues -
Disease features -
Remarks -