hereditary coproporphyria
Human disease
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hereditary coproporphyria
Summary
hereditary coproporphyria is a rare disease[1]. It draws 39 Wikipedia views per month (rare_disease category, ranking #204 of 627).[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's subclass of is recorded as porphyria due to ALAD deficiency[5].
- hereditary coproporphyria's subclass of is recorded as disease[6].
- hereditary coproporphyria's MeSH descriptor ID is recorded as D046349[7].
- hereditary coproporphyria's OMIM ID is recorded as 121300[8].
- hereditary coproporphyria's ICD-9 ID is recorded as 277.1[9].
- hereditary coproporphyria's DiseasesDB is recorded as 30591[10].
- hereditary coproporphyria's Freebase ID is recorded as /m/02ktkt[11].
- hereditary coproporphyria's MeSH tree code is recorded as C06.552.830.074[12].
- hereditary coproporphyria's MeSH tree code is recorded as C16.320.850.742.074[13].
- hereditary coproporphyria's MeSH tree code is recorded as C17.800.827.742.074[14].
- hereditary coproporphyria's MeSH tree code is recorded as C18.452.811.400.074[15].
- hereditary coproporphyria's eMedicine ID is recorded as 205374[16].
- hereditary coproporphyria's Disease Ontology ID is recorded as DOID:13269[17].
- hereditary coproporphyria's Orphanet ID is recorded as 79273[18].
- hereditary coproporphyria's NCI Thesaurus ID is recorded as C84759[19].
- hereditary coproporphyria's health specialty is recorded as endocrinology[20].
- hereditary coproporphyria's genetic association is recorded as CPOX[21].
- hereditary coproporphyria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_13269[22].
- hereditary coproporphyria's exact match is recorded as http://identifiers.org/doid/DOID:13269[23].
- hereditary coproporphyria's UMLS CUI is recorded as C0162531[24].
- hereditary coproporphyria's ICD-10-CM is recorded as E80.29[25].
- hereditary coproporphyria's PatientsLikeMe condition ID is recorded as hereditary-coproporphyria[26].
- hereditary coproporphyria's GARD rare disease ID is recorded as 6619[27].
Why It Matters
hereditary coproporphyria draws 39 Wikipedia views per month (rare_disease category, ranking #204 of 627).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] It is known by 8 alternative names across languages and contexts.[29]