Disease #00862 (Vohwinkel syndrome with ichthyosis, OMIM:604117)

Official abbreviation -
Name Vohwinkel syndrome with ichthyosis
OMIM ID 604117
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene LOR
Associated tissues -
Disease features -
Remarks -

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