|
distal arthrogryposis type 2B3 (Sheldon-Hall)
|
32751 |
|
|
lymphedema, hereditary, type 1C
|
13278 |
|
|
frontonasal dysplasia type 3
|
13271 |
|
|
hyperoxaluria, primary, type 3
|
13327 |
|
|
primary hyperoxaluria type 3
|
13327 |
|
|
phakomatosis pigmentovascularis type 3
|
19327 |
|
|
amelogenesis imperfecta, type 3c
|
32717 |
|
|
hyperoxaluria, primary, type III
|
13327 |
|
|
primary hyperoxaluria type III
|
13327 |
|
|
hyperoxaluria, primary, type III; HP3
|
http://purl.obolibrary.org/obo/MONDO_0013327 |
|
|
neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia
|
32758 |
|
|
generalized epilepsy with febrile seizures plus, type 10
|
32777 |
|
|
mitochondrial disease with hypertrophic cardiomyopathy
|
16327 |
|
