|
retinitis pigmentosa type 51
|
13274 |
|
|
lymphedema, hereditary, type 1C
|
13278 |
|
|
polydactyly, postaxial, type a10
|
32785 |
|
|
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 |
|
