monilethrix
Human disease
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monilethrix
Summary
monilethrix is a rare disease[1]. monilethrix draws 114 Wikipedia views per month (rare_disease category, ranking #193 of 627).[2]
Key Facts
- monilethrix's instance of is recorded as rare disease[3].
- monilethrix's instance of is recorded as class of disease[4].
- monilethrix is a type of autosomal dominant disease[5].
- monilethrix is a type of hair diseases[6].
- monilethrix is a type of isolated genetic hair shaft abnormality[7].
- monilethrix's Commons category is recorded as Monilethrix[8].
- monilethrix's NCI Thesaurus ID is recorded as C84894[9].
- monilethrix's health specialty is recorded as medical genetics[10].
- monilethrix's genetic association is recorded as KRT86[11].
- monilethrix's genetic association is recorded as KRT83[12].
- monilethrix's genetic association is recorded as KRT81[13].
- monilethrix's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050472[14].
- monilethrix's exact match is recorded as http://identifiers.org/doid/DOID:0050472[15].
- monilethrix's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_573[16].
- monilethrix's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
monilethrix draws 114 Wikipedia views per month (rare_disease category, ranking #193 of 627).[2] monilethrix has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[18] monilethrix is known by 10 alternative names across languages and contexts.[19]