|
glycogen storage disease caused by mutation in LDHA
|
13047 |
|
|
glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
|
13047 |
|
|
glycogen storage disease due to muscle beta-enolase deficiency
|
13046 |
|
|
glycogen storage disease 13
|
13046 |
|
|
glycogen storage disease type 11
|
13047 |
|
|
glycogen storage disease type 13
|
13046 |
|
|
glycogen storage disease XI
|
13047 |
|
|
glycogen storage disease XI; GSD11
|
http://purl.obolibrary.org/obo/MONDO_0013047 |
|
|
glycogen storage disease XIII
|
13046 |
|
|
glycogen storage disease XIII; GSD13
|
http://purl.obolibrary.org/obo/MONDO_0013046 |
|
|
auditory cortex disorders
|
D001304 |
|
|
hypertensive renal disease, benign
|
1304 |
|
|
hypertensive renal disease, benign, without mention of renal failure
|
1304 |
|
|
auditory pathway disorders, central
|
D001304 |
|
