Riley-Day syndrome
hereditary sensory and autonomic neuropathy type III (HSAN-III), is a disorder of the autonomic nervous system which affects the development and survival of sensory
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Riley-Day syndrome
Summary
Riley-Day syndrome is a class of disease[1]. It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Riley-Day syndrome's instance of is recorded as class of disease[3].
- Riley-Day syndrome is a type of hereditary sensory and autonomic neuropathy[4].
- Riley-Day syndrome is a type of primary orthostatic hypotension[5].
- Riley-Day syndrome is a type of rare genetic developmental defect during embryogenesis[6].
- Riley-Day syndrome is a type of other dermis disorder[7].
- Riley-Day syndrome is a type of other genetic dermis disorder[8].
- Riley-Day syndrome is a type of nervous system anomaly with eye involvement[9].
- Riley-Day syndrome is a type of autosomal recessive hereditary sensory and autonomic neuropathy[10].
- Riley-Day syndrome is a type of disease[11].
- Riley-Day syndrome's Commons category is recorded as Familial dysautonomia[12].
- Riley-Day syndrome's NCI Thesaurus ID is recorded as C84706[13].
- Riley-Day syndrome's health specialty is recorded as neurology[14].
- Riley-Day syndrome's genetic association is recorded as ELP1[15].
- Riley-Day syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_11589[16].
- Riley-Day syndrome's exact match is recorded as http://identifiers.org/doid/DOID:11589[17].
- Riley-Day syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1764[18].
- Riley-Day syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
Riley-Day syndrome has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2] It is known by 28 alternative names across languages and contexts.[20]