|
t-cell immunodeficiency, congenital alopecia, and nail dystrophy
|
C536781 |
|
|
glossopharyngeal nerve cranial nerve palsy
|
2781 |
|
|
immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist
|
7815 |
|
|
NAD(P)HX epimerase deficiency
|
20781 |
|
|
terminal 7p deletion (del 7p21-p22) chromosome 7
|
C537818 |
|
|
insulin-dependent, 24 diabetes mellitus
|
C567818 |
|
|
oral facial digital syndrome, type IX
|
C557818 |
|
|
Helicobacter pylori disease or disorder
|
6781 |
|
|
atypical dentin dysplasia due to SMOC2 deficiency
|
17819 |
|
|
encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1
|
20781 |
|
|
lymphoproliferative syndrome, ebv-associated, autosomal, 1
|
C567815 |
|
|
congenital hypotonia, epilepsy, developmental delay, and digital anomalies
|
32781 |
|
