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Heinz body anemia
human disease
HEINZ BODY ANEMIAS
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Statements
instance of
class of disease
0 references
subclass of
congenital hemolytic anemia
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007705
congenital nonspherocytic hemolytic anemia
1 reference
stated in
Disease Ontology
retrieved
27 November 2020
Disease Ontology ID
DOID:0111363
autosomal dominant disease
1 reference
stated in
Disease Ontology
retrieved
27 November 2020
Disease Ontology ID
DOID:0111363
symptoms and signs
Heinz body
0 references
genetic association
HBA2
1 reference
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000188536/MONDO_0007705
based on heuristic
inferred from an Open Targets association score over 0.7
HBB
1 reference
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000244734/MONDO_0007705
based on heuristic
inferred from an Open Targets association score over 0.7
exact match
http://purl.obolibrary.org/obo/HP_0005511
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0005511
http://www.orpha.net/ORDO/Orphanet_178330
0 references
http://purl.obolibrary.org/obo/DOID_0111363
1 reference
stated in
Disease Ontology
retrieved
27 November 2020
Disease Ontology ID
DOID:0111363
http://identifiers.org/doid/DOID:0111363
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
MeSH descriptor ID
C563030
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007705
C563030
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0005511
Disease Ontology ID
DOID:0111363
1 reference
stated in
Disease Ontology
retrieved
27 November 2020
Disease Ontology ID
DOID:0111363
GARD rare disease ID
10718
0 references
Human Phenotype Ontology ID
HP:0005511
2 references
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007705
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0005511
ICD-10-CM
D58.2
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007705
ICD-11 (foundation)
561612692
0 references
Mondo ID
MONDO_0007705
0 references
OMIM ID
140700
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007705
Orphanet ID
178330
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007705
UMLS CUI
C0700299
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0007705
C0700299
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0005511
UniProt disease ID
DI-01698
0 references
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Wikiquote
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Wikisource
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Wikiversity
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Wikivoyage
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Wiktionary
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