|
isolated corpus callosum agenesis
|
9022 |
|
|
punctata, rhizomelic chondrodysplasia
|
D018902 |
|
|
punctatas, rhizomelic chondrodysplasia
|
D018902 |
|
|
rhizomelic form chondrodysplasia punctata
|
D018902 |
|
|
aortopulmonary septal defect
|
21902 |
|
|
nerve injuries, auriculotemporal
|
D000080902 |
|
|
nerve injury, auriculotemporal
|
D000080902 |
|
|
osteopetrosis (disease), autosomal recessive
|
19026 |
|
|
brain stem capillary hemangioblastoma
|
3902 |
|
|
MST1R nasopharyngeal carcinoma
|
http://purl.obolibrary.org/obo/MONDO_0014902 |
|
|
autosomal dominant deafness 27
|
12902 |
|
|
hereditary motor and sensory neuropathy with agenesis of the corpus callosum
|
902 |
|
|
adenoma, hepatocellular, benign
|
18902 |
|
|
nasopharyngeal carcinoma caused by mutation in MST1R
|
http://purl.obolibrary.org/obo/MONDO_0014902 |
|
