hereditary coproporphyria
Human disease
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hereditary coproporphyria
Summary
hereditary coproporphyria is a rare disease[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- hereditary coproporphyria's instance of is recorded as rare disease[3].
- hereditary coproporphyria's instance of is recorded as class of disease[4].
- hereditary coproporphyria is a type of porphyria due to ALAD deficiency[5].
- hereditary coproporphyria is a type of disease[6].
- hereditary coproporphyria's NCI Thesaurus ID is recorded as C84759[7].
- hereditary coproporphyria's health specialty is recorded as endocrinology[8].
- hereditary coproporphyria's genetic association is recorded as CPOX[9].
- hereditary coproporphyria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_13269[10].
- hereditary coproporphyria's exact match is recorded as http://identifiers.org/doid/DOID:13269[11].
- hereditary coproporphyria's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
hereditary coproporphyria has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[13]