a rare genetic neurodevelopmental disorder
Attributes | Values |
---|---|
rdf:type | |
owl:sameAs | |
description |
|
exact match | |
exact match | |
health specialty | |
Mondo ID | |
DiseasesDB | |
Disease Ontology ID | |
Mondo ID | |
Disease Ontology ID | |
health specialty | |
Mondo ID |
|
DiseasesDB |
|
Disease Ontology ID |
|
rdfs:label |
|
skos:prefLabel |
|
name |
|
Freebase ID | |
Freebase ID |
|
instance of | |
instance of | |
subclass of | |
subclass of | |
KEGG ID | |
KEGG ID | |
KEGG ID |
|
Orphanet ID | |
genetic association |
|
ICD-10-CM | |
PatientsLikeMe condition ID | |
GARD rare disease ID | |
OMIM ID |