inclusion-cell disease
Human disease
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inclusion-cell disease
Summary
inclusion-cell disease is a developmental defect during embryogenesis[1]. It draws 61 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #97 of 308).[2]
Key Facts
- inclusion-cell disease's instance of is recorded as developmental defect during embryogenesis[3].
- inclusion-cell disease's instance of is recorded as rare disease[4].
- inclusion-cell disease's instance of is recorded as class of disease[5].
- inclusion-cell disease is a type of rare genetic developmental defect during embryogenesis[6].
- inclusion-cell disease is a type of lysosomal storage disease with skeletal involvement[7].
- inclusion-cell disease is a type of mucolipidosis[8].
- inclusion-cell disease is a type of disease[9].
- inclusion-cell disease's NCI Thesaurus ID is recorded as C61270[10].
- inclusion-cell disease's health specialty is recorded as endocrinology[11].
- inclusion-cell disease's genetic association is recorded as GNPTAB[12].
- inclusion-cell disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080070[13].
- inclusion-cell disease's exact match is recorded as http://identifiers.org/doid/DOID:0080070[14].
- inclusion-cell disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_576[15].
- inclusion-cell disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
inclusion-cell disease draws 61 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #97 of 308).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[17] It is known by 14 alternative names across languages and contexts.[18]