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Alport syndrome (Q1331116)

Item Discussion
monogenic disease characterized by glomerulonephritis, endstage kidney disease, and hearing loss
  • hereditary nephritis
  • nephritis, familial
  • familial nephritis
  • Alport's syndrome
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Language Label Description Also known as
British English
Alport syndrome
monogenic disease characterized by glomerulonephritis, endstage kidney disease, and hearing loss
  • hereditary nephritis
  • nephritis, familial
  • familial nephritis
  • Alport's syndrome

Statements

Freebase ID
/m/036b8w
1 reference
stated in
Q15241312 (Deleted Item)
publication date
28 October 2013
Disease Ontology ID
DOID:10983
1 reference
stated in
Disease Ontology English
retrieved
18 Ocak 2022
Disease Ontology ID
DOID:10983
subclass of
monogenic disease English
1 reference
stated in
Disease Ontology English
retrieved
18 Ocak 2022
Disease Ontology ID
DOID:10983
Q200779 (Deleted Item)
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
MonDO ID
MONDO:0005334
Q1054718 (Deleted Item)
0 references
Q179630 (Deleted Item)
1 reference
stated in
Disease Ontology English
retrieved
18 Ocak 2022
Disease Ontology ID
DOID:10983
Q112193769 (Deleted Item)
0 references
health speciality
Q1071953 (Deleted Item)
0 references
Commons category
Alport syndrome
0 references
UMLS CUI English
C0027706
1 reference
stated in
Disease Ontology English
retrieved
15 Mayıs 2019
Disease Ontology ID
DOID:10983
Quora topic ID
Alport-Syndrome
1 reference
stated in
Q51711 (Deleted Item)
JSTOR topic ID
hereditary-nephritis
0 references
Orphanet ID
63
1 reference
stated in
Disease Ontology English
retrieved
15 Mayıs 2019
Disease Ontology ID
DOID:10983
instance of
Q42303753 (Deleted Item)
1 reference
reference URL
https://ddrare.nibiohn.go.jp/
retrieved
17 Mayıs 2019
Q112193867 (Deleted Item)
0 references
WikiSkripta ID English
20710
0 references
GARD rare disease ID
5785
1 reference
stated in
Disease Ontology English
retrieved
15 Mayıs 2019
Disease Ontology ID
DOID:10983
BabelNet ID
03596859n
1 reference
stated in
BabelNet
NCI Thesaurus ID English
C34842
0 references
MeSH
D009394
mapping relation type English
exact match English
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
MonDO ID
MONDO:0005334
MonDO ID
MONDO:0005334
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
MonDO ID
MONDO:0005334
MeSH Code
C12.706.742
0 references
C12.777.419.570.620
0 references
C13.351.875.742
0 references
C13.351.968.419.570.620
0 references
C16.131.939.742
0 references
C17.300.200.517
0 references
Gran Enciclopèdia Catalana ID
0002949
0 references
Microsoft Academic ID
2776908417
0 references
2908747133
0 references
named after
Q708901 (Deleted Item)
0 references
KEGG ID English
H00581
0 references
ICD-11 (foundation) English
1170919425
0 references
Genetics Home Reference Conditions ID English
alport-syndrome
0 references
symptoms and signs English
Q605006 (Deleted Item)
0 references
Q373597 (Deleted Item)
0 references
Q16035842 (Deleted Item)
0 references
kidney failure
0 references
National Library of Israel J9U ID
987007294888205171
1 reference
stated in
Q188915 (Deleted Item)
Encyclopedia of China ID (Third Edition) English
170900
0 references
P11143 (Deleted Property)
Alport syndrome Property P11143 not found, cannot determine the data type to use.
0 references
 
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