rare genetic 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 |
|
instance of | |
instance of | |
subclass of | |
subclass of | |
Orphanet ID | |
ICD-9-CM | |
genetic association | |
ICD-10-CM | |
PatientsLikeMe condition ID | |
GARD rare disease ID | |
OMIM ID | |
Orphanet ID |
|
ICD-9-CM |
|
genetic association | |
ICD-10-CM |
|
PatientsLikeMe condition ID |
|
GARD rare disease ID |
|
OMIM ID |
|
ICD-9 ID | |
ICD-9 ID |
|
skos:altLabel |
|
NCI Thesaurus ID | |
BabelNet ID | |
UMLS CUI | |
MeSH descriptor ID | |
on focus list of Wikimedia project | |
Microsoft Academic ID | |
MeSH tree code | |
DeCS ID | |
BabelNet ID | |
MeSH descriptor ID |