About: Mowat-Wilson syndrome

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rare genetic disorder

Attributes	Values
rdf:type	Item
owl:sameAs	Mowat-Wilson syndrome
description	Krankheit (de) مرض يصيب الإنسان (ar) хвороба (uk) enfermedad humana (es) malattia genetica rara (it) rare genetic disorder (en)
exact match	wds:Q2757585-1660B072-9863-4EFB-B8C3-36B433CDFE38 wds:Q2757585-BA989AB6-054B-401F-A91A-FDB8233A64E8
exact match	http://purl.obolibrary.org/obo/DOID_0060485 http://identifiers.org/doid/DOID:0060485
Mondo ID	wds:Q2757585-44634BB6-A362-42B0-851E-832B839BC509
DiseasesDB	wds:q2757585-72359A3E-AA92-494B-A746-DE9CFD5228FD
Disease Ontology ID	wds:Q2757585-15F67E21-A3A7-463D-8476-D0FD174E16C5
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0009341
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:0060485
Mondo ID	MONDO_0009341
DiseasesDB	32975
Disease Ontology ID	DOID:0060485
rdfs:label	Mowat-Wilson syndrome (en) Mowat-Wilson syndrome (nl) Mowat-Wilson sendromu (tr) Mowat-Wilson-Syndrom (de) Mowat–Wilson syndrome (en-ca) Mowat–Wilson syndrome (en-gb) Mowat–Wilson-szindróma (hu) Mowat–Wilsonin oireyhtymä (fi) Síndrome de Mowat-Wilson (es) Zespół Mowata-Wilsona (pl) sindrome di Mowat-Wilson (it) syndrome de Mowat-Wilson (fr) متلازمة موات ويلسون (ar)
skos:prefLabel	Mowat-Wilson syndrome (en) Mowat-Wilson syndrome (nl) Mowat-Wilson sendromu (tr) Mowat-Wilson-Syndrom (de) Mowat–Wilson syndrome (en-ca) Mowat–Wilson syndrome (en-gb) Mowat–Wilson-szindróma (hu) Mowat–Wilsonin oireyhtymä (fi) Síndrome de Mowat-Wilson (es) Zespół Mowata-Wilsona (pl) sindrome di Mowat-Wilson (it) syndrome de Mowat-Wilson (fr) متلازمة موات ويلسون (ar)
name	Mowat-Wilson syndrome (en) Mowat-Wilson syndrome (nl) Mowat-Wilson sendromu (tr) Mowat-Wilson-Syndrom (de) Mowat–Wilson syndrome (en-ca) Mowat–Wilson syndrome (en-gb) Mowat–Wilson-szindróma (hu) Mowat–Wilsonin oireyhtymä (fi) Síndrome de Mowat-Wilson (es) Zespół Mowata-Wilsona (pl) sindrome di Mowat-Wilson (it) syndrome de Mowat-Wilson (fr) متلازمة موات ويلسون (ar)
Freebase ID	wds:Q2757585-47B7FC92-EE55-4A30-A8CD-2C995BE3E2BE
Freebase ID	/m/0f785g
instance of	wds:Q2757585-815071EA-3727-4DCC-BA71-BE6932D5BAE2 wds:Q2757585-B2C89223-0BD2-419E-8F42-FBA8ACF20822 wds:Q2757585-D17235C7-2838-45A8-AB64-18D15C13E053 wds:Q2757585-F4718E65-A46C-4869-8A03-4A15DE9E6EEE
instance of	class of disease rare disease designated intractable/rare disease developmental defect during embryogenesis
subclass of	wds:Q2757585-2448245B-49A4-4CCF-BCCB-E88CBE0FDD5C wds:Q2757585-437EBF6D-1052-42CD-A0F8-B18F48579758 wds:Q2757585-444411dc-4134-a5e1-1094-faa8a417da3e wds:Q2757585-4F25637D-3A55-47AE-B46A-F1282F8BCFF3 wds:Q2757585-5EA19BEB-FA10-4C9E-A35F-09ADB1BF62CC wds:Q2757585-E8423879-DFB1-46DC-935F-056970CD4BFF
subclass of	genetic disease syndrome Hirschsprung's disease multiple congenital anomalies/dysmorphic syndrome-intellectual disability genetic syndromic intellectual disability syndromic intestinal malformation
KEGG ID	wds:Q2757585-7A3EBD2F-7B19-436A-9150-7958281F7A4F
KEGG ID	http://www.kegg.jp/entry/H00908
KEGG ID	H00908
UniProt disease ID	wds:Q2757585-670c2f2b-4e3a-d896-8b1b-3a99c81d81a3
Orphanet ID	wds:Q2757585-55C1BFF1-6837-4234-A6CB-79BDD9D75FB4
ICD-9-CM	wds:Q2757585-53BBAFE2-C872-4175-B67F-0AD67C0939AA
genetic association	wds:Q2757585-67E248B6-EBD7-481A-9CFC-5CDB7A6AD371
ICD-10-CM	wds:Q2757585-F1A21145-BAD8-4B1E-9518-9EF1BD7F60DE
PatientsLikeMe condition ID	wds:Q2757585-614a7497-4295-a501-bade-ae603b8b4c6f
GARD rare disease ID	wds:Q2757585-186A6E8B-DA9F-4865-805E-17D1BA852447
OMIM ID	wds:Q2757585-1A48B21F-1B25-4264-9C04-B60555C330BD
Genetics Home Reference Conditions ID	wds:Q2757585-6C5BAB15-2FC8-4361-A99C-A771BB804101
UniProt disease ID	DI-01749
Orphanet ID	2152
ICD-9-CM	759.89
genetic association	ZEB2
ICD-10-CM	Q43.1
PatientsLikeMe condition ID	mowat-wilson-syndrome
GARD rare disease ID	9673

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