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About:
Galloway-Mowat syndrome
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Class
subClassOf
syndrome
label
Galloway-Mowat syndrome
(en)
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0080694
database_cross_reference
GARD:65
MESH:C537548
NCI:C132195
OMIM:PS251300
ORDO:2065
SNOMEDCT_US_2021_09_01:721297008
UMLS_CUI:C0795949
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
A syndrome that is characterized by developmental delay, progressive microcephaly, cerebral and cerebellar atrophy with extrapyramidal involvement, and optic atrophy.
is
subClassOf
of
Galloway-Mowat syndrome 1
Galloway-Mowat syndrome 2
Galloway-Mowat syndrome 3
Galloway-Mowat syndrome 4
Galloway-Mowat syndrome 5
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50941454
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