OBO ID: DOID:4621 |
Term Name: | holoprosencephaly | Search Ontology: | |
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Synonyms: |
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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. (2) | ||
References: |
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Ontology: | Human Disease ( DOID:4621 ) |
OTHER holoprosencephaly PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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cyp26a1rw716/rw716 | standard conditions | Gongal et al., 2008 |
WT + MO1-tgif1 | standard conditions | Gongal et al., 2008 |
uq05jgTg | standard conditions | Periyasamy et al., 2019 |
PHENOTYPE
No data available
CITATIONS (4)
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