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(Q3338681)
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English
Hereditary sensory and autonomic neuropathy type I
medical condition
HSAN I
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Statements
instance of
rare disease
0 references
class of disease
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subclass of
hereditary sensory and autonomic neuropathy
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health specialty
neurology
0 references
genetic association
SPTLC1
1 reference
stated in
Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I
Identifiers
ICD-11 (foundation)
1989773046
0 references
ICD-11 ID (MMS)
8C21.0
subject named as
Hereditary sensory and autonomic neuropathy type I
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Microsoft Academic ID
2777189886
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OMIM ID
162400
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Orphanet ID
36386
0 references
WikiProjectMed ID
Hereditary sensory and autonomic neuropathy type I
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Sitelinks
Wikipedia
(4 entries)
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arwiki
الاعتلال العصبي الحسي الذاتي الوراثي من النوع الأول
dewiki
Acropathia ulcero-mutilans familiaris
enwiki
Hereditary sensory and autonomic neuropathy type I
frwiki
Neuropathie héréditaire sensitive et autonomique de type I
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