|
infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
|
33864 |
|
|
pure red-cell aplasia of adults
|
20338 |
|
|
striatal Necrosis, bilateral, and progressive polyneuropathy
|
13382 |
|
|
spinal muscular atrophy caused by mutation in ATP7A
|
10338 |
|
|
spinal muscular atrophy, distal, X-linked 3
|
10338 |
|
|
spinal muscular atrophy, distal, X-linked 3; SMAX3
|
http://purl.obolibrary.org/obo/MONDO_0010338 |
|
|
spinal muscular atrophy, distal, X-linked recessive
|
10338 |
|
|
spinal muscular atrophy, distal, X-linked type 3
|
10338 |
|
|
myocardial (rhabdomyomas and fibromas) tumor
|
D006338 |
|
|
myocardial (rhabdomyomas and fibromas) tumors
|
D006338 |
|
|
veno-occlusive disease and immunodeficiency syndrome
|
9338 |
|
|
limb deficiencies, and ossification defects of skull diaphragmatic defects
|
C563380 |
|
|
contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
|
8338 |
|
|
autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect
|
33850 |
|
