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English
retinitis pigmentosa 61
retinitis pigmentosa that has material basis in mutation in the CLRN1 gene on chromosome 3q25
RP61
Retinitis Pigmentosa type 61
RETINITIS PIGMENTOSA 61; RP61
RETINITIS PIGMENTOSA 61
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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
30 November 2020
Disease Ontology ID
DOID:0110373
genetic disease
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:0110373
genetic association
CLRN1
2 references
stated in
UniProt
UniProt protein ID
P58418
retrieved
13 August 2019
stated in
CLRN1 mutations cause nonsyndromic retinitis pigmentosa
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0110373
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0110373
http://identifiers.org/doid/DOID:0110373
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
Disease Ontology ID
DOID:0110373
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0110373
ICD-10-CM
H35.5
2 references
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110373
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0013610
Mondo ID
MONDO_0013610
0 references
OMIM ID
614180
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0110373
UMLS CUI
C3280041
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0013610
UniProt disease ID
DI-03234
0 references
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Wikiversity
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Wiktionary
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Multilingual sites
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