Disease #01264 (coproporphyria, hereditary, OMIM:121300)

Official abbreviation -
Name coproporphyria, hereditary
OMIM ID 121300
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 7
Phenotype entries for this disease 6
Associated with 1 gene CPOX
Associated tissues -
Disease features -
Remarks -


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00183216 - - - - - - - - 0 - - coproporphyria, hereditary - CPOX CPOX 1 1 Manuel Mendez
00183384 - - - - - - - - 0 - - coproporphyria, hereditary - CPOX CPOX 1 1 Manuel Mendez
00183387 - - - - - - - - 0 - - coproporphyria, hereditary - CPOX CPOX 1 1 Manuel Mendez
00183397 - - - - - - - - 0 - - coproporphyria, hereditary - CPOX CPOX 1 1 Manuel Mendez
00183398 - - - - - - - - 0 - - coproporphyria, hereditary - CPOX CPOX 1 1 Manuel Mendez
00183399 - - - - - - - - 0 - - coproporphyria, hereditary - CPOX CPOX 1 1 Manuel Mendez
00183400 - - - - - - - - 0 - - coproporphyria, hereditary - CPOX CPOX 1 1 Manuel Mendez
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