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Peters anomaly
Human disease
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Statements
instance of
rare disease
0 references
class of disease
0 references
subclass of
corneal disease
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0060673
anterior segment mesenchymal dysgenesis
0 references
genetic disease
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:0060673
health specialty
medical genetics
0 references
genetic association
PAX6
determination method
mouse model
1 reference
stated in
Reduced expression of Pax6 in lens and cornea of mutant mice leads to failure of chamber angle development and juvenile glaucoma.
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0060673
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0060673
http://identifiers.org/doid/DOID:0060673
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://purl.obolibrary.org/obo/HP_0000659
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000659
Identifiers
MeSH descriptor ID
C537884
subject named as
Peters anomaly
2 references
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060673
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000659
KEGG ID
H01075
0 references
Disease Ontology ID
DOID:0060673
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0060673
GARD rare disease ID
7377
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060673
Human Phenotype Ontology ID
HP:0000659
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000659
ICD-10-CM
Q13.4
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060673
ICD-11 (foundation)
1902926622
0 references
OMIM ID
604229
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060673
Orphanet ID
708
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060673
ScienceDirect topic ID
medicine-and-dentistry/peters-anomaly
0 references
nursing-and-health-professions/peters-anomaly
0 references
pharmacology-toxicology-and-pharmaceutical-science/peters-anomaly
0 references
UMLS CUI
C0344559
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0000659
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Wikiversity
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Wikivoyage
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Wiktionary
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