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(Q56014420)
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English
Axenfeld anomaly
No description defined
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Statements
instance of
class of disease
0 references
subclass of
goniodysgenesis
0 references
genetic association
FOXC1
1 reference
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000054598/MONDO_0020368
based on heuristic
inferred from an Open Targets association score over 0.7
ICD-9-CM
743.44
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0020368
exact match
http://www.orpha.net/ORDO/Orphanet_98978
0 references
Identifiers
ICD-10-CM
Q15.0
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0020368
Mondo ID
MONDO_0020368
0 references
Orphanet ID
98978
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0020368
UMLS CUI
C0266548
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0020368
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