microvillus inclusion disease
Human disease
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microvillus inclusion disease
Summary
microvillus inclusion disease is a rare disease[1]. It draws 36 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2]
Key Facts
- microvillus inclusion disease's instance of is recorded as rare disease[3].
- microvillus inclusion disease's instance of is recorded as class of disease[4].
- microvillus inclusion disease is a type of congenital diarrhea[5].
- microvillus inclusion disease is a type of congenital enteropathy involving intestinal mucosa development[6].
- microvillus inclusion disease is a type of intractable diarrhea of infancy[7].
- microvillus inclusion disease is a type of genetic disease[8].
- microvillus inclusion disease is a type of autosomal recessive disease[9].
- microvillus inclusion disease's ICD-9-CM is recorded as 579.8[10].
- microvillus inclusion disease's genetic association is recorded as MYO5B[11].
- microvillus inclusion disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060775[12].
- microvillus inclusion disease's exact match is recorded as http://identifiers.org/doid/DOID:0060775[13].
- microvillus inclusion disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2290[14].
- microvillus inclusion disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
microvillus inclusion disease draws 36 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2] It is known by 21 alternative names across languages and contexts.[16]