mucolipidosis type IV
Lysosomal storage disease
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mucolipidosis type IV
Summary
mucolipidosis type IV is a rare disease[1]. It draws 33 Wikipedia views per month (rare_disease category, ranking #207 of 627).[2]
Key Facts
- mucolipidosis type IV's instance of is recorded as rare disease[3].
- mucolipidosis type IV's instance of is recorded as developmental defect during embryogenesis[4].
- mucolipidosis type IV's instance of is recorded as class of disease[5].
- mucolipidosis type IV's subclass of is recorded as rare genetic epilepsy[6].
- mucolipidosis type IV's subclass of is recorded as lysosomal disease with epilepsy[7].
- mucolipidosis type IV's subclass of is recorded as metabolic disease with corneal opacity[8].
- mucolipidosis type IV's subclass of is recorded as unclassified primitive or secondary maculopathy[9].
- mucolipidosis type IV's subclass of is recorded as hereditary retinal dystrophy[10].
- mucolipidosis type IV's subclass of is recorded as rare genetic developmental defect during embryogenesis[11].
- mucolipidosis type IV's subclass of is recorded as mucolipidosis[12].
- mucolipidosis type IV's OMIM ID is recorded as 252650[13].
- mucolipidosis type IV's ICD-10 ID is recorded as E75.1[14].
- mucolipidosis type IV's DiseasesDB is recorded as 32693[15].
- mucolipidosis type IV's KEGG ID is recorded as H00144[16].
- mucolipidosis type IV's GeneReviews ID is recorded as NBK1214[17].
- mucolipidosis type IV's Disease Ontology ID is recorded as DOID:0080490[18].
- mucolipidosis type IV's Orphanet ID is recorded as 578[19].
- mucolipidosis type IV's NCI Thesaurus ID is recorded as C84896[20].
- mucolipidosis type IV's health specialty is recorded as endocrinology[21].
- mucolipidosis type IV's genetic association is recorded as MCOLN1[22].
- mucolipidosis type IV's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_578[23].
- mucolipidosis type IV's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080490[24].
- mucolipidosis type IV's exact match is recorded as http://identifiers.org/doid/DOID:0080490[25].
- mucolipidosis type IV's UMLS CUI is recorded as C0238286[26].
- mucolipidosis type IV's ICD-10-CM is recorded as E75.1[27].
Why It Matters
mucolipidosis type IV draws 33 Wikipedia views per month (rare_disease category, ranking #207 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It is known by 9 alternative names across languages and contexts.[29]