Preferred Name |
neutropenia, severe congenital, 1, autosomal dominant |
|
Synonyms |
neutropenia, severe congenital, 1, autosomal dominant neutropenia, severe congenital 1, autosomal dominant SCN1 |
|
ID |
http://purl.obolibrary.org/obo/MONDO_0042490 |
|
has_exact_synonym |
neutropenia, severe congenital, 1, autosomal dominant neutropenia, severe congenital 1, autosomal dominant |
|
has_related_synonym |
SCN1 |
|
IAO_0000233 | ||
label |
neutropenia, severe congenital, 1, autosomal dominant |
|
prefixIRI |
MONDO:0042490 |
|
prefLabel |
neutropenia, severe congenital, 1, autosomal dominant |
|
subClassOf |
Create mapping
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.obolibrary.org/obo/MONDO_0042490 | MONDO | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0042490 | EFO | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0042490 | MONDO | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0042490 | EFO | LOOM | |
http://purl.bioontology.org/ontology/OMIM/202700 | OMIM | LOOM | |
http://identifiers.org/omim/202700 | REXO | LOOM | |
http://identifiers.org/omim/202700 | GEXO | LOOM | |
http://identifiers.org/omim/202700 | RETO | LOOM |