SHMARQL

hereditary sensory and autonomic neuropathy

<http://www.wikidata.org/entity/Q3702898>

congenital disorder of nervous system
rdfs:label
"hereditary sensory and autonomic neuropathy"@en
skos:altLabel
"HSAN"@en
"Hereditary sensory and autonomic neuropathy (disorder)"@en
"amilial dysautonomia, type II"@en
"congenital insensitivity to pain"@en
"familial dysautonomia, type II"@en
"hereditary sensory neuropathy"@en
schema:description
"congenital disorder of nervous system"@en
schema:dateModified "2026-10-23T23:24:01+00:00"^^xsd:dateTime
schema:version 2560154060
wikibase:identifiers 24
wikibase:sitelinks 5
wikibase:statements 49
p:P14914 wd:statement/Q3702898-B3860045-6FDF-4468-B6EE-C86700F0A12B
p:P1550 wd:statement/Q3702898-2a4b4a04-4702-690e-6d31-7d7ad02d482f
p:P1995 wd:statement/Q3702898-844B17AF-7C5B-4EED-A28E-C2E1DEE7105C
p:P2293 wd:statement/Q3702898-14892995-23F1-4900-83D5-5A3360FD45E3
wd:statement/Q3702898-1C7C3E1A-16F9-4FC3-B3AB-8B82F7007209
wd:statement/Q3702898-20B783E4-3EBF-4FE7-A539-31425F3B2D97
wd:statement/Q3702898-3A59B725-F8B1-4BD2-B130-3257FEFAB6A5
wd:statement/Q3702898-3E26B6C2-A7A4-4BC6-A98B-D354E0748244
wd:statement/Q3702898-44488475-F01A-4B6B-9E2C-E236E798A189
wd:statement/Q3702898-4D7FDA95-0F6B-4364-AE98-65D0C70091E3
wd:statement/Q3702898-57076D63-4F61-449E-96B2-7A20A058466F
wd:statement/Q3702898-6DAB1EF0-35B7-4406-A91A-E04B240D9C06
wd:statement/Q3702898-74ED27EF-DD00-4CDE-A18B-EB0B463B6C09
wd:statement/Q3702898-7964F950-F06A-45E9-A3EB-CEB2775F00E0
wd:statement/Q3702898-87380099-001E-48B7-AAC2-3994A7ACFCF3
wd:statement/Q3702898-8AB3FC01-59A3-4C53-8057-1662736E0AE3
wd:statement/Q3702898-95CF26A3-2DC0-4E3D-8F09-2DB22A0F159B
wd:statement/Q3702898-A7587B38-4703-4B65-986F-CA98B7C227CD
wd:statement/Q3702898-A922D5EF-B4C7-4467-B5FD-1B798FAE1D8B
wd:statement/Q3702898-CC63E781-63EE-45D2-86B9-16923D3AF6AA
wd:statement/Q3702898-EC8F4FF6-EC81-4BC1-8960-98F6930273DB
p:P279 wd:statement/Q3702898-2dc3f053-4740-2fc6-b029-39a3ea84cc9c
wd:statement/Q3702898-ae6a02d9-4e55-a4ca-8bd7-7924dcd294f7
p:P2888 wd:statement/Q3702898-2A8095B9-E066-498B-A9C7-269944664E28
wd:statement/Q3702898-5FFFC440-449D-433C-9A5B-5C7DBE90E2F2
p:P31 wd:statement/Q3702898-1BEFFCDF-2A26-473F-89A6-D0FC77486F24
p:P4317 wd:statement/Q3702898-23B02FAB-2F48-4B4E-A7ED-AB0A529F9F67
wd:statement/Q3702898-3DDD618F-599E-4912-8355-9582C4813FBF
p:P486 wd:statement/Q3702898-e973f970-41d9-19b5-052a-7d4728edcb6d
p:P492 wd:statement/Q3702898-5DE4F8AB-2D89-4C09-B93E-CBC91A30F604
p:P493 wd:statement/q3702898-719CAF74-00A7-4649-960B-BF9DBCB0A17E
p:P5008 wd:statement/Q3702898-01DA309E-CA3C-4DBD-B4F4-D1D98C7BAB9D
p:P557 wd:statement/q3702898-3C5409DE-8D4E-4DE6-A409-A8F8E1E2758F
wd:statement/q3702898-69A10236-5812-44DB-B57B-020DC8A547B7
wd:statement/q3702898-A362020E-6260-44B8-A020-FED4B1052F0B
wd:statement/q3702898-AA1E8EE5-24C8-4542-9E21-B5349E6F41D8
wd:statement/q3702898-D7F27402-0529-49C5-8E19-9B4745F24D4C
p:P6366 wd:statement/Q3702898-1DBFB25B-1362-440E-80A7-ACA100E6390A
wd:statement/Q3702898-DBEF2307-963A-4F1D-8535-F1F0679F393E
p:P665 wd:statement/Q3702898-2B76A874-882F-40A1-B2F0-9095B2F2F363
p:P672 wd:statement/Q3702898-080efce1-45a4-de74-ed1c-5b5c2b605469
wd:statement/Q3702898-274b24af-48b5-d049-7808-0f275e7024b0
wd:statement/Q3702898-2a463667-453c-2cc6-17fe-d321e245c7cb
wd:statement/Q3702898-41601c75-4dbd-b9fe-1776-5d3a9b2fa0c1
wd:statement/Q3702898-e31f16f4-4743-22e1-49e3-625617b02596
p:P699 wd:statement/Q3702898-008708FF-33F4-41F5-BAF7-DCC96A96C342
p:P7329 wd:statement/Q3702898-728117a1-b62a-4893-8405-cfa41997ec8b
p:P7464 wd:statement/Q3702898-F69454D8-1E4B-4580-B0E5-5219BDEA39E6
p:P7807 wd:statement/Q3702898-CBC00C2A-F8D2-4A52-8F27-DF422DAE834A
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D009477>
p:direct-normalized/P6366 <https://makg.org/entity/2778405720>
<https://makg.org/entity/2911010462>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00265>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C10.500.250>
<http://id.nlm.nih.gov/mesh/C10.574.500.493>
<http://id.nlm.nih.gov/mesh/C10.668.829.800.175>
<http://id.nlm.nih.gov/mesh/C16.131.666.310>
<http://id.nlm.nih.gov/mesh/C16.320.400.415>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050548>
wdt:P14914 "D140471"
wdt:P1550 "140471"
wdt:P1995 neurology
wdt:P2293 NGF
NTRK1
SCN9A
DNMT1
SCN11A
KIF1A
AIFM1
CRLF1
SPTLC2
SPTLC1
CLCF1
ATL3
ATL1
RETREG1
KLHL7
PRDM12
WNK1
DST
wdt:P279 hereditary disorder
peripheral neuropathy
wdt:P2888 <http://identifiers.org/doid/DOID:0050548>
<http://purl.obolibrary.org/obo/DOID_0050548>
wdt:P31 type of disease
wdt:P4317 "12267"
"12688"
wdt:P486 "D009477"
wdt:P492 "162400"
wdt:P493 "356.2"
wdt:P5008 WikiProject Medicine
wdt:P557 "11631"
"32096"
"32097"
"32501"
"32610"
wdt:P6366 "2778405720"
"2911010462"
wdt:P665 "H00265"
wdt:P672 "C10.500.250"
"C10.574.500.493"
"C10.668.829.800.175"
"C16.131.666.310"
"C16.320.400.415"
wdt:P699 "DOID:0050548"
wdt:P7329 "8C21"
wdt:P7464 "familial-dysautonomia"
wdt:P7807 "1091217288"
Download as:
TurtleJSON-LDRDF/XML
data from SPARQL profile: Wikidata