Preferred Name | holoprosencephaly 2 | |
Synonyms |
HPE2 |
|
Definitions |
A holoprosencephaly that has_material_basis_in mutation in the homeobox-containing SIX3 gene on chromosome 2p21. |
|
ID |
http://purl.obolibrary.org/obo/DOID_0110872 |
|
alternative label |
HPE2 |
|
database_cross_reference |
OMIM:157170 MESH:C563579 |
|
definition |
A holoprosencephaly that has_material_basis_in mutation in the homeobox-containing SIX3 gene on chromosome 2p21. |
|
has exact synonym |
HPE2 |
|
has material basis in | ||
has_obo_namespace |
disease_ontology |
|
id |
DOID:0110872 |
|
label |
holoprosencephaly 2 |
|
notation |
DOID:0110872 |
|
note |
A holoprosencephaly that has_material_basis_in mutation in the homeobox-containing SIX3 gene on chromosome 2p21. |
|
preferred label |
holoprosencephaly 2 |
|
prefLabel |
holoprosencephaly 2 |
|
subClassOf |
Create mapping