|
limb-girdle muscular dystrophy due to FKRP deficiency
|
11787 |
|
|
limb-girdle muscular dystrophy type 2I
|
11787 |
|
|
susceptibility to familial meningioma
|
11789 |
|
|
ALG12-congenital disorder of glycosylation
|
11783 |
|
|
congenital disorder of glycosylation type 1g
|
11783 |
|
|
congenital disorder of glycosylation type Ig
|
11783 |
|
|
Perenial allergic rhinitis
|
http://purl.obolibrary.org/obo/MONDO_0011786 |
|
|
congenital disorder of glycosylation, type Ig
|
11783 |
|
|
congenital disorder of glycosylation, type Ig; CDG1G
|
http://purl.obolibrary.org/obo/MONDO_0011783 |
|
|
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 |
|
|
autosomal dominant spastic paraplegia type 19
|
11785 |
|
