Disease #01979 (OODD (dysplasia, odontoonychodermal (OODD)), OMIM:257980)

Official abbreviation OODD
Name dysplasia, odontoonychodermal (OODD)
OMIM ID 257980
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene WNT10A
Associated tissues -
Disease features -
Remarks -

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