Disease #00967 (Bowen-Conradi syndrome, OMIM:211180)

Official abbreviation -
Name Bowen-Conradi syndrome
OMIM ID 211180
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene EMG1
Associated tissues -
Disease features -
Remarks -

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