Preferred Name | holoprosencephaly | |
Synonyms |
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Definitions |
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. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
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ID |
http://purl.obolibrary.org/obo/DOID_4621 |
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comment |
Xref MGI. OMIM mapping confirmed by DO. [SN]. |
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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. |
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hasDbXref |
MESH:D016142 ICD10CM:Q04.2 UMLS_CUI:C0079541 NCI:C74988 ORDO:2162 SNOMEDCT_US_2016_03_01:30915001 SNOMEDCT_US_2016_03_01:44519006 |
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hasExactSynonym |
Holoprosencephaly sequence (disorder) |
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hasOBONamespace |
disease_ontology |
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id |
DOID:4621 |
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imported from | ||
inSubset | ||
label |
holoprosencephaly |
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prefixIRI |
DOID:4621 |
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prefLabel |
holoprosencephaly |
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subClassOf |
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