|
hereditary papillary carcinoma of the kidney
|
3789 |
|
|
cutaneous syndactyly of fingers and toes, and jejunal atresia asymmetrical coronal synostosis
|
C537890 |
|
|
waardenburg-shah syndrome, neurologic variant
|
C563789 |
|
|
peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease
|
C563789 |
|
|
phenol sulfotransferase deficiency
|
C537895 |
|
|
transfusion reaction due to serum protein reaction
|
43789 |
|
|
carbohydrate deficient glycoprotein syndrome type
|
13789 |
|
|
carbohydrate deficient glycoprotein syndrome type Ir
|
13789 |
|
|
congenital disorder of glycosylation type 1r
|
13789 |
|
|
congenital disorder of glycosylation type Ir
|
13789 |
|
|
congenital disorder of glycosylation, type Ir
|
13789 |
|
|
congenital disorder of glycosylation, type Ir; CDG1R
|
http://purl.obolibrary.org/obo/MONDO_0013789 |
|
|
hereditary papillary renal carcinoma
|
3789 |
|
