|
muscular dystrophy, limb-girdle, type 2I
|
11787 |
|
|
monosomy 7 myelodysplasia and leukemia syndrome
|
31178 |
|
|
ALG12-congenital disorder of glycosylation
|
11783 |
|
|
congenital disorder of glycosylation type 1g
|
11783 |
|
|
congenital disorder of glycosylation type Ig
|
11783 |
|
|
congenital disorder of glycosylation, type Ig
|
11783 |
|
|
congenital disorder of glycosylation, type Ig; CDG1G
|
http://purl.obolibrary.org/obo/MONDO_0011783 |
|
|
allergic form of rhinitis
|
11786 |
|
|
spinal, quadriplegic paralysis
|
D011782 |
|
|
hereditary spastic paraplegia 19
|
11785 |
|
|
hereditary spastic paraplegia type 19
|
11785 |
|
|
paralysis, spinal, quadriplegic
|
D011782 |
|
|
FKRP autosomal recessive limb-girdle muscular dystrophy
|
11787 |
|
|
Perenial allergic rhinitis
|
http://purl.obolibrary.org/obo/MONDO_0011786 |
|
|
autosomal dominant spastic paraplegia 19
|
11785 |
|
