|
MSRB3 autosomal recessive nonsyndromic deafness
|
13386 |
|
|
deafness, autosomal recessive type 74
|
13386 |
|
|
vertigo, episodic recurrent
|
D020338 |
|
|
vertigos, episodic recurrent
|
D020338 |
|
|
vestibular neuritides, recurrent
|
D020338 |
|
|
vestibular neuritis, recurrent
|
D020338 |
|
|
acquired pure red cell aplasia
|
20338 |
|
|
adult pure red cell aplasia
|
20338 |
|
|
idiopathic pure red cell aplasia
|
20338 |
|
|
adult pure red-cell aplasia
|
20338 |
|
|
neuropathy, hereditary sensory, type 1D
|
13381 |
|
|
neuropathy, hereditary sensory, type ID
|
13381 |
|
|
neuropathy, hereditary sensory, type ID; HSN1D
|
http://purl.obolibrary.org/obo/MONDO_0013381 |
|
|
X-linked distal spinal muscular atrophy type 3
|
10338 |
|
