Jump to:
loading...| Preferred Name |
Autosomal_Dominant_Hereditary_Disorder |
|
| Synonyms |
|
|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Autosomal_Dominant_Hereditary_Disorder |
|
| ID |
C98829 |
|
| NCI_Definition |
An inherited disorder that manifests when one copy of a mutated gene is present. |
|
| NCI_PT |
Autosomal Dominant Inherited Disorder |
|
| NICHD_Definition |
_ |
|
| prefixIRI |
Autosomal_Dominant_Hereditary_Disorder |
|
| prefLabel |
Autosomal_Dominant_Hereditary_Disorder |
|
| Subset_Association1 |
NICHD Pediatric Terminology |
|
| Subset_Association2 |
Neonatal Research Network Terminology |
|
| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Genetic_Disorder |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/SNOMEDCT/11164009 | SNOMEDCT | LOOM |