| Metadata | |
|---|---|
| ID | DOID:4621 |
| Name | holoprosencephaly |
| 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. http://en.wikipedia.org/wiki/Holoprosencephaly, http://www.ncbi.nlm.nih.gov/books/NBK1530/ |
| Xrefs |
SNOMEDCT_US_2023_03_01:30915001 |
| Subsets |
DO_rare_slim NCIthesaurus |
| Synonyms |
Holoprosencephaly sequence [EXACT] |
| Parent Relationships |
is_a syndrome |
| Subclass Logical Relationships |
disease has basis in some symptom |