Disease #01084 (CKS (syndrome, CK (CKS)), OMIM:300831)

Official abbreviation CKS
Name syndrome, CK (CKS)
OMIM ID 300831
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NSDHL
Associated tissues -
Disease features X-linked recessive
Remarks -