mucolipidosis type IV
Lysosomal storage disease
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mucolipidosis type IV
Summary
mucolipidosis type IV is a rare disease[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[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 is a type of rare genetic epilepsy[6].
- mucolipidosis type IV is a type of lysosomal disease with epilepsy[7].
- mucolipidosis type IV is a type of metabolic disease with corneal opacity[8].
- mucolipidosis type IV is a type of unclassified primitive or secondary maculopathy[9].
- mucolipidosis type IV is a type of hereditary retinal dystrophy[10].
- mucolipidosis type IV is a type of rare genetic developmental defect during embryogenesis[11].
- mucolipidosis type IV is a type of mucolipidosis[12].
- mucolipidosis type IV's NCI Thesaurus ID is recorded as C84896[13].
- mucolipidosis type IV's health specialty is recorded as endocrinology[14].
- mucolipidosis type IV's genetic association is recorded as MCOLN1[15].
- mucolipidosis type IV's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_578[16].
- mucolipidosis type IV's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080490[17].
- mucolipidosis type IV's exact match is recorded as http://identifiers.org/doid/DOID:0080490[18].
- mucolipidosis type IV's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
mucolipidosis type IV has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 9 alternative names across languages and contexts.[20]