Disease #06336 (OFD15 (?Orofaciodigital syndrome XV), OMIM:617127)

Official abbreviation OFD15
Name ?Orofaciodigital syndrome XV
OMIM ID 617127
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene KIAA0753
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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