|
osteoarthritis susceptibility 3
|
11923.0 |
|
|
caudal DUPLICATION anomaly
|
11928 |
|
|
laminin alpha-2 deficiency
|
11925 |
|
|
autosomal recessive deafness 18A
|
11192 |
|
|
autosomal dominant deafness 48
|
11920 |
|
|
chromosome 1p36 deletion syndrome
|
11929 |
|
|
aural atresia, congenital; CAA
|
http://purl.obolibrary.org/obo/MONDO_0011921 |
|
|
MYO1A autosomal dominant nonsyndromic deafness
|
11920 |
|
|
subtelomeric 1p36 deletion
|
11929 |
|
|
deafness, autosomal dominant type 48
|
11920 |
|
|
nonimmune chronic idiopathic neutropenia of adults
|
11922 |
|
|
LAMA2-related muscular dystrophy
|
11925 |
|
|
congenital muscular dystrophy caused by mutation in LAMA2
|
11925 |
|
|
congenital muscular dystrophy due to laminin alpha2 deficiency
|
11925 |
|
