Preferred Name |
holoprosencephaly |
|
Synonyms |
Holoprosencephaly sequence |
|
Definitions |
Xref MGI. OMIM mapping confirmed by DO. [SN]. A congenital nervous system abnormality characterized by failed or incomplete separation of the forebrain early in gestation; it is accompanied by a spectrum of characteristic craniofacial anomalies. |
|
ID |
http://purl.obolibrary.org/obo/DOID_4621 |
|
comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
|
database_cross_reference |
MESH:D016142 ICD10CM:Q04.2 SNOMEDCT_US_2023_03_01:30915001 UMLS_CUI:C0079541 MIM:PS236100 GARD:6665 NCI:C74988 ORDO:2162 |
|
definition |
A congenital nervous system abnormality characterized by failed or incomplete separation of the forebrain early in gestation; it is accompanied by a spectrum of characteristic craniofacial anomalies. |
|
disease has basis in | ||
has exact synonym |
Holoprosencephaly sequence |
|
has_obo_namespace |
disease_ontology |
|
id |
DOID:4621 |
|
in_subset | ||
label |
holoprosencephaly |
|
notation |
DOID:4621 |
|
prefLabel |
holoprosencephaly |
|
subClassOf |