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loading...| Preferred Name |
Holoprosencephaly_Sequence |
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| Synonyms |
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| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Holoprosencephaly_Sequence |
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| ID |
C74988 |
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| NCI_Definition |
A rare disorder characterized by the failure of the forebrain to divide into distinct hemispheres. It is associated with craniofacial abnormalities, developmental abnormalities, and seizures. |
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| NCI_PT |
Holoprosencephaly |
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| NICHD_Definition |
_ |
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| prefixIRI |
Holoprosencephaly_Sequence |
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| prefLabel |
Holoprosencephaly_Sequence |
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| Subset_Association1 |
NICHD Pediatric Terminology |
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| Subset_Association2 |
Neonatal Research Network Terminology |
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| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Abnormality_of_the_Nervous_System |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://radlex.org/RID/RID34733 | RADLEX | LOOM | |
| http://purl.bioontology.org/ontology/SNMI/D4-01520 | SNMI | LOOM | |
| http://purl.bioontology.org/ontology/SNOMEDCT/30915001 | SNOMEDCT | LOOM |