Preferred Name |
Meckel-Gruber_Syndrome |
|
Synonyms |
|
|
ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Meckel-Gruber_Syndrome |
|
ID |
C98978 |
|
NCI_Definition |
A rare, lethal, autosomal recessive inherited syndrome characterized by pulmonary hypoplasia, central nervous system malformations, and hepatic malformations. |
|
NCI_PT |
Meckel-Gruber Syndrome |
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NICHD_Definition |
_ |
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prefixIRI |
Meckel-Gruber_Syndrome |
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prefLabel |
Meckel-Gruber_Syndrome |
|
Subset_Association1 |
NICHD Pediatric Terminology |
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Subset_Association2 |
Neonatal Research Network Terminology |
|
SYN | ||
subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Genetic_Disorder |
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