McLeod syndrome
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McLeod syndrome
Summary
McLeod syndrome is a designated intractable/rare disease[1]. It draws 1,066 Wikipedia views per month (designated_intractable_rare_disease category, ranking #54 of 201).[2]
Key Facts
- McLeod syndrome's instance of is recorded as designated intractable/rare disease[3].
- McLeod syndrome's instance of is recorded as rare disease[4].
- McLeod syndrome's instance of is recorded as class of disease[5].
- McLeod syndrome is a type of neuroacanthocytosis[6].
- McLeod syndrome is a type of nervous system heredodegenerative disease[7].
- McLeod syndrome is a type of rare genetic epilepsy[8].
- McLeod syndrome is a type of neurometabolic disease[9].
- McLeod syndrome is a type of constitutional hemolytic anemia due to acanthocytosis[10].
- McLeod syndrome is a type of syndrome associated with dilated cardiomyopathy[11].
- McLeod syndrome is a type of other metabolic disease with epilepsy[12].
- McLeod syndrome is a type of X-linked disease[13].
- McLeod syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4051[14].
- McLeod syndrome's ICD-9-CM is recorded as 289.89[15].
- McLeod syndrome's different from is recorded as Swyer-James syndrome[16].
- McLeod syndrome's genetic association is recorded as XK[17].
- McLeod syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_59306[18].
- McLeod syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0112107[19].
- McLeod syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0112107[20].
Why It Matters
McLeod syndrome draws 1,066 Wikipedia views per month (designated_intractable_rare_disease category, ranking #54 of 201).[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[21] It is known by 13 alternative names across languages and contexts.[22]