|
retinal, 1, north carolina type macular dystrophy
|
C537835 |
|
|
malignant hyperthermia of anesthesia caused by mutation in RYR1
|
7783 |
|
|
ALG12-congenital disorder of glycosylation
|
11783 |
|
|
congenital disorder of glycosylation type 1g
|
11783 |
|
|
congenital disorder of glycosylation type 1n
|
12783 |
|
|
congenital disorder of glycosylation type Ig
|
11783 |
|
|
congenital disorder of glycosylation type In
|
12783 |
|
|
congenital disorder of glycosylation, type Ig
|
11783 |
|
|
congenital disorder of glycosylation, type Ig; CDG1G
|
http://purl.obolibrary.org/obo/MONDO_0011783 |
|
|
congenital disorder of glycosylation, type In
|
12783 |
|
|
congenital disorder of glycosylation, type In; CDG1N
|
http://purl.obolibrary.org/obo/MONDO_0012783 |
|
|
progressive external ophthalmoplegia with cerebellar ataxia infantile
|
9783 |
|
|
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
|
9783 |
|
|
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1; PEOB1
|
http://purl.obolibrary.org/obo/MONDO_0009783 |
|
|
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 1
|
9783 |
|
