|
Charcot-Marie-Tooth disease recessive intermediate B
|
13338 |
|
|
Charcot-Marie-Tooth disease, recessive intermediate B
|
13338 |
|
|
Charcot-Marie-Tooth neuropathy recessive intermediate B
|
13338 |
|
|
Charcot-Marie-Tooth disease, recessive intermediate B; CMTRIB
|
http://purl.obolibrary.org/obo/MONDO_0013338 |
|
|
Charcot-Marie-Tooth disease recessive intermediate b
|
13338.0 |
|
|
Charcot-Marie-Tooth disease recessive intermediate type B
|
13338 |
|
|
Charcot-Marie-Tooth disease, recessive intermediate, B
|
13338 |
|
|
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 |
|
