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loading...| Preferred Name |
Autosomal_Recessive_Hereditary_Disorder |
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| Synonyms |
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|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Autosomal_Recessive_Hereditary_Disorder |
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| ID |
C85866 |
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| NCI_Definition |
An inherited disorder manifested only when two copies of a mutated gene are present. |
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| NCI_PT |
Autosomal Recessive Inherited Disorder |
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| NICHD_Definition |
_ |
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| prefixIRI |
Autosomal_Recessive_Hereditary_Disorder |
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| prefLabel |
Autosomal_Recessive_Hereditary_Disorder |
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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#Genetic_Disorder |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://sbmi.uth.tmc.edu/ontology/ochv#C0265388 | OCHV | LOOM | |
| http://purl.bioontology.org/ontology/SNOMEDCT/85995004 | SNOMEDCT | LOOM |