Disease #00373 (CED4 (dysplasia, cranioectodermal, type 4 (CED-4)), OMIM:614378)

Official abbreviation CED4
Name dysplasia, cranioectodermal, type 4 (CED-4)
OMIM ID 614378
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene WDR19
Associated tissues -
Disease features -
Remarks -

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