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Metadata
ID DOID:13269
Name hereditary coproporphyria
Xrefs

GARD:6619

ICD10CM:E80.29

MESH:D046349

MIM:121300

NCI:C84759

SNOMEDCT_US_2023_03_01:7425008

UMLS_CUI:C0162531

Subsets

DO_rare_slim

NCIthesaurus

Synonyms

Coproporphyrinogen oxidase deficiency [EXACT]

hereditary coproporphyria porphyria [EXACT]

Parent Relationships

is_a acute porphyria

is_a digenic disease

Subclass Logical Relationships

has material basis in some digenic inheritance

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