|
WOLFRAM-like syndrome, autosomal dominant; WFSL
|
http://purl.obolibrary.org/obo/MONDO_0013673 |
|
|
neurodegeneration with brain iron accumulation 4
|
13674 |
|
|
neurodegeneration with brain iron accumulation 4; NBIA4
|
http://purl.obolibrary.org/obo/MONDO_0013674 |
|
|
neurodegeneration with brain iron accumulation caused by mutation in C19orf12
|
13674 |
|
|
neurodegeneration with brain iron accumulation due to C19orf12 mutation
|
13674 |
|
|
neurodegeneration with brain iron accumulation type 4
|
13674 |
|
|
sclerosteosis caused by mutation in LRP4
|
13679 |
|
|
keratoconus with cataract
|
13678 |
|
|
congestive splenomegaly, chronic
|
1367 |
|
|
Accelerated phase chronic myeloid leukemia
|
21367 |
|
|
hydatidiform Mole, complete
|
13671 |
|
|
chromosome 15q25 deletion syndrome
|
13672 |
|
|
TMEM43 autosomal dominant Emery-Dreifuss muscular dystrophy
|
13677 |
|
|
multiple mitochondrial dysfunctions syndrome 2
|
13675 |
|
|
multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia
|
13675 |
|
