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(Q27677803)
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English
retinitis pigmentosa 36
retinitis pigmentosa that has material basis in mutation in the PRCD gene on chromosome 17q25
RP36
retinitis pigmentosa type 36
RETINITIS PIGMENTOSA 36; RP36
RETINITIS PIGMENTOSA 36
RP 36
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Statements
instance of
rare disease
0 references
class of disease
0 references
subclass of
retinitis pigmentosa
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0110405
genetic disease
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:0110405
genetic association
PRCD
2 references
stated in
UniProt
UniProt protein ID
Q00LT1
retrieved
13 August 2019
stated in
Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0110405
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0110405
http://identifiers.org/doid/DOID:0110405
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
MeSH descriptor ID
C566431
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0012523
Disease Ontology ID
DOID:0110405
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0110405
GARD rare disease ID
10403
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0012523
ICD-10-CM
H35.5
2 references
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110405
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0012523
Mondo ID
MONDO_0012523
0 references
OMIM ID
610599
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110405
UMLS CUI
C1864621
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0012523
UniProt disease ID
DI-02263
0 references
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Wikiversity
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