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(Q55789215)
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English
goniodysgenesis
human disease
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Statements
instance of
class of disease
0 references
subclass of
secondary dysgenetic glaucoma associated with neural crest cell migration anomaly
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0020218
exact match
http://www.orpha.net/ORDO/Orphanet_98633
0 references
Identifiers
Mondo ID
MONDO_0020218
0 references
Orphanet ID
98633
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0020218
UMLS CUI
C0311237
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0020218
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