Preferred Name | hypochondroplasia | |
Synonyms |
|
|
Definitions |
An osteochondrodysplasia that has_material_basis_in mutation in the FGFR3 gene which affects ossification of cartilage and results_in short limb dwarfism. |
|
ID |
http://purl.obolibrary.org/obo/DOID_0080041 |
|
database_cross_reference |
ICD10CM:Q77.4 UMLS_CUI:C0410529 MESH:C562937 NCI:C118697 SNOMEDCT_US_2023_03_01:205468002 GARD:6724 MIM:146000 ORDO:429 |
|
definition |
An osteochondrodysplasia that has_material_basis_in mutation in the FGFR3 gene which affects ossification of cartilage and results_in short limb dwarfism. |
|
has material basis in | ||
has_obo_namespace |
disease_ontology |
|
id |
DOID:0080041 |
|
in_subset | ||
label |
hypochondroplasia |
|
notation |
DOID:0080041 |
|
note |
An osteochondrodysplasia that has_material_basis_in mutation in the FGFR3 gene which affects ossification of cartilage and results_in short limb dwarfism. |
|
preferred label |
hypochondroplasia |
|
prefLabel |
hypochondroplasia |
|
subClassOf |
Create mapping