Disease #01083 (CHILD (CHILD syndrome), OMIM:308050)

Official abbreviation CHILD
Name CHILD syndrome
OMIM ID 308050
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 -
Remarks -