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loading...| Preferred Name |
Neurocutaneous_Syndrome |
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| Synonyms |
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| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Neurocutaneous_Syndrome |
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| ID |
C84348 |
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| NCI_Definition |
A hereditary syndrome affecting the central nervous system that is associated with lesions of the skin and retina. Representative examples include neurofibromatosis, tuberous sclerosis, von Hippel-Lindau syndrome, and Sturge-Weber syndrome. |
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| NCI_PT |
Phakomatosis |
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| NICHD_Definition |
_ |
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| prefixIRI |
Neurocutaneous_Syndrome |
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| prefLabel |
Neurocutaneous_Syndrome |
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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 |
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