|
MHC class II expression deficiency
|
8855 |
|
|
burnett Schwartz Berberian syndrome
|
18855 |
|
|
SCID, HLA CLASS II-NEGATIVE BARE lymphocyte syndrome, type II, complementation group A, included
|
8855 |
|
|
SCID, HLA Class 2-negative
|
8855 |
|
|
SCID, HLA Class II-negative
|
8855 |
|
|
major histocompatibility complex class II expression deficiency
|
8855 |
|
|
amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2
|
18855 |
|
|
severe combined immunodeficiency, HLA Class II-negative
|
8855 |
|
|
severe combined immunodeficiency, HLA class ii-negative
|
8855 |
|
|
keratosis pilaris atrophicans
|
18855 |
|
|
keratosis pilaris atrophicans facies
|
18855 |
|
|
keratosis pilaris atrophicans; KPA
|
http://purl.obolibrary.org/obo/MONDO_0018855 |
|
|
immunodeficiency by defective expression of HLA class 2
|
8855 |
|
|
immunodeficiency by defective expression of HLA class type 2
|
8855 |
|
