monomelic amyotrophy
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monomelic amyotrophy
Summary
monomelic amyotrophy is a class of disease[1]. It draws 72 Wikipedia views per month (class_of_disease category, ranking #560 of 1,968).[2]
Key Facts
- monomelic amyotrophy's instance of is recorded as class of disease[3].
- monomelic amyotrophy's subclass of is recorded as genetic motor neuron disease[4].
- monomelic amyotrophy's subclass of is recorded as acquired motor neuron disease[5].
- monomelic amyotrophy's MeSH descriptor ID is recorded as C538253[6].
- monomelic amyotrophy's OMIM ID is recorded as 602440[7].
- monomelic amyotrophy's pseudonym is recorded as Hirayama disease[8].
- monomelic amyotrophy's Orphanet ID is recorded as 65684[9].
- monomelic amyotrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_65684[10].
- monomelic amyotrophy's UMLS CUI is recorded as C1865384[11].
- monomelic amyotrophy's ICD-10-CM is recorded as G12.8[12].
- monomelic amyotrophy's PatientsLikeMe condition ID is recorded as monomelic-amyotrophy[13].
- monomelic amyotrophy's GARD rare disease ID is recorded as 9697[14].
- monomelic amyotrophy's Mondo ID is recorded as MONDO_0011224[15].
- monomelic amyotrophy's Microsoft Academic ID is recorded as 2778831127[16].
- monomelic amyotrophy's ICD-11 ID is recorded as 8B60.6[17].
- monomelic amyotrophy's ICD-11 ID is recorded as 2090347823[18].
- monomelic amyotrophy's WikiProjectMed ID is recorded as Monomelic amyotrophy[19].
- monomelic amyotrophy's Experimental Factor Ontology ID is recorded as 1001989[20].
Why It Matters
monomelic amyotrophy draws 72 Wikipedia views per month (class_of_disease category, ranking #560 of 1,968).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[21] It is known by 9 alternative names across languages and contexts.[22]