|
congenital disorder OF glycosylation, type IIo; CDG2O
|
http://purl.obolibrary.org/obo/MONDO_0014789 |
|
|
corpus callosum, agenesis OF, with FACIAL anomalies and cerebellar ataxia
|
14787 |
|
|
corpus callosum, agenesis OF, with FACIAL anomalies and cerebellar ataxia; CCAFCA
|
http://purl.obolibrary.org/obo/MONDO_0014787 |
|
|
corpus callosum, agenesis of, with Facial anomalies and cerebellar ataxia
|
14787 |
|
|
odontogenic keratocysts, and skeletal anomalies multiple basal cell nevi
|
D001478 |
|
|
nevus syndrome, basal cell
|
D001478 |
|
|
nasopharyngeal neoplasm, benign
|
21478 |
|
|
glycosylphosphatidylinositol biosynthesis defect 12
|
14780 |
|
|
growth and developintellectual disability, ocular ptosis, cardiac defect, and anal atresia
|
11478 |
|
|
severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome
|
14784 |
|
|
growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia
|
11478 |
|
