|
autoimmune thyroid disease, susceptibility to, 4
|
11983.0 |
|
|
non-syndromic synpolydactyly caused by mutation in FBLN1
|
11984 |
|
|
cone-rod dystrophy caused by mutation in RPGRIP1
|
11987 |
|
|
post kala-Azar dermal leishmaniasis
|
11989 |
|
|
immunodeficiency with hyper IgM type 4
|
11985 |
|
|
obsolete rare genetic disease
|
21198.0 |
|
|
immunodeficiency with hyper-IgM type 4
|
11985 |
|
|
immunodeficiency with hyper-IgM, type 4
|
11985 |
|
|
immunodeficiency with hyper-IgM, type 4; HIGM4
|
http://purl.obolibrary.org/obo/MONDO_0011985 |
|
|
tropical calcific pancreatitis
|
11986 |
|
|
post-kala-azar dermal leishmaniasis
|
11989 |
|
|
Missouri type of spondyloepimetaphyseal dysplasia
|
11198 |
|
|
spondyloepimetaphyseal dysplasia type 2
|
11198 |
|
