Attributes | Values |
---|---|
rdf:type | |
exact match | |
exact match | |
Mondo ID | |
Mondo ID | |
Mondo ID |
|
rdfs:label |
|
skos:prefLabel |
|
name |
|
instance of | |
instance of | |
subclass of | |
subclass of | |
UniProt disease ID | |
Orphanet ID | |
genetic association | |
ICD-10-CM | |
GARD rare disease ID | |
OMIM ID | |
Genetics Home Reference Conditions ID | |
UniProt disease ID |
|
Orphanet ID |
|
genetic association | |
ICD-10-CM |
|
GARD rare disease ID |
|
OMIM ID |
|
Genetics Home Reference Conditions ID |
|
skos:altLabel |
|
NCI Thesaurus ID | |
UMLS CUI | |
MeSH descriptor ID | |
ICD-11 ID (MMS) | |
ICD-11 (foundation) | |
MeSH descriptor ID | |
NCI Thesaurus ID |
|
UMLS CUI |
|
MeSH descriptor ID |
|
ICD-11 ID (MMS) |
|
ICD-11 (foundation) |
|
is about of | |
is cites work of | |
is cites work of | |
is genetic association of | |
is genetic association of | |
is established from medical condition of | |
is established from medical condition of |