|
mfm, desmin-related myofibrillar myopathy, desmin-related
|
C563319 |
|
|
myofibrillar, desmin-related myopathy
|
C563319 |
|
|
desmin-related myofibrillar myopathy, desmin-related mfm
|
C563319 |
|
|
autosomal recessive nonsyndromic deafness 106
|
33198 |
|
|
autosomal recessive nonsyndromic deafness 107
|
33199 |
|
|
obsolete skin/hair/eye pigmentation, variation in
|
33196.0 |
|
|
deafness, autosomal recessive 106
|
33198 |
|
|
deafness, autosomal recessive 106; DFNB106
|
http://purl.obolibrary.org/obo/MONDO_0033198 |
|
|
deafness, autosomal recessive 107
|
33199 |
|
|
deafness, autosomal recessive 107; DFNB107
|
http://purl.obolibrary.org/obo/MONDO_0033199 |
|
|
chromosome 4Q32.1-q32.2 triplication syndrome
|
13319 |
|
