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Human Disease and Mouse Model Detail
Human Disease Porphyria Cutanea Tarda
OMIM ID: 176100
Human Phenotype Ontology associations
Synonyms PCT; PCT, 'Familial' Type; Pct, Type II; Porphyria; Porphyria Cutanea Tarda, Type II; Porphyria, Hepatocutaneous Type; Uroporphyrinogen Decarboxylase Deficiency
View all models View ALL (1) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     HFE* Hfe View 1 model HomoloGene and HGNC
UROD* Urod View 1 model HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory