|
slowed nerve conduction velocity, autosomal dominant; SNCV
|
http://purl.obolibrary.org/obo/MONDO_0011998 |
|
|
autosomal recessive deafness 38
|
11991 |
|
|
autosomal dominant deafness 41
|
11994 |
|
|
ossicle chain disarticulation
|
1199 |
|
|
ossicle chain discontinuity
|
1199 |
|
|
P2RX2 autosomal dominant nonsyndromic deafness
|
11994 |
|
|
deafness, autosomal dominant type 41
|
11994 |
|
|
deafness, autosomal dominant 41
|
11994 |
|
|
deafness, autosomal dominant 41; DFNA41
|
http://purl.obolibrary.org/obo/MONDO_0011994 |
|
|
dislocation of ear ossicle
|
1199 |
|
|
dislocation of ear ossicles
|
1199 |
|
|
chronic granulocytic leukemia
|
11996 |
|
|
chronic myelogenous leukemia, BCR-ABL1 Positive
|
11996 |
|
|
chronic myelogenous leukemia, BCR-ABL1 positive
|
11996 |
|
