neurogenic arthrogryposis multiplex congenita

Summary

neurogenic arthrogryposis multiplex congenita is a rare disease^[1]. It draws 261 Wikipedia views per month (rare_disease category, ranking #87 of 627).^[2]

Key Facts

• neurogenic arthrogryposis multiplex congenita's instance of is recorded as rare disease^[3].
• neurogenic arthrogryposis multiplex congenita's instance of is recorded as developmental defect during embryogenesis^[4].
• neurogenic arthrogryposis multiplex congenita's instance of is recorded as class of disease^[5].
• neurogenic arthrogryposis multiplex congenita's subclass of is recorded as neurological disorder^[6].
• neurogenic arthrogryposis multiplex congenita's subclass of is recorded as arthrogryposis^[7].
• neurogenic arthrogryposis multiplex congenita's subclass of is recorded as genetic nervous system disorder^[8].
• neurogenic arthrogryposis multiplex congenita's subclass of is recorded as arthrogryposis multiplex congenita^[9].
• neurogenic arthrogryposis multiplex congenita's subclass of is recorded as genetic disease^[10].
• neurogenic arthrogryposis multiplex congenita's subclass of is recorded as autosomal recessive disease^[11].
• neurogenic arthrogryposis multiplex congenita's subclass of is recorded as disease^[12].
• neurogenic arthrogryposis multiplex congenita's Commons category is recorded as Arthrogryposis multiplex congenita^[13].
• neurogenic arthrogryposis multiplex congenita's MeSH descriptor ID is recorded as C536614^[14].
• neurogenic arthrogryposis multiplex congenita's OMIM ID is recorded as 617468^[15].
• neurogenic arthrogryposis multiplex congenita's OMIM ID is recorded as 208100^[16].
• neurogenic arthrogryposis multiplex congenita's ICD-9 ID is recorded as 728.3^[17].
• neurogenic arthrogryposis multiplex congenita's ICD-9 ID is recorded as 754.89^[18].
• neurogenic arthrogryposis multiplex congenita's DiseasesDB is recorded as 31688^[19].
• neurogenic arthrogryposis multiplex congenita's DiseasesDB is recorded as 31816^[20].
• neurogenic arthrogryposis multiplex congenita's Freebase ID is recorded as /m/0nrd_^[21].
• neurogenic arthrogryposis multiplex congenita's KEGG ID is recorded as H02358^[22].
• neurogenic arthrogryposis multiplex congenita's ICPC 2 ID is recorded as L82^[23].
• neurogenic arthrogryposis multiplex congenita's eMedicine ID is recorded as 941917^[24].
• neurogenic arthrogryposis multiplex congenita's Disease Ontology ID is recorded as DOID:0090124^[25].
• neurogenic arthrogryposis multiplex congenita's topic's main category is recorded as Category:Arthrogryposis^[26].
• neurogenic arthrogryposis multiplex congenita's Gran Enciclopèdia Catalana ID is recorded as 0080959^[27].

Why It Matters

neurogenic arthrogryposis multiplex congenita draws 261 Wikipedia views per month (rare_disease category, ranking #87 of 627).^[2] It has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.^[28] It is known by 33 alternative names across languages and contexts.^[29]