Disease #01282 (Dermatopathia pigmentosa reticularis, OMIM:125595)

Official abbreviation -
Name Dermatopathia pigmentosa reticularis
OMIM ID 125595
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 KRT14
Associated tissues -
Disease features -
Remarks -

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