|
primary t-cell immunodeficiency disorders
|
C536780 |
|
|
t cell immunodeficiency primary
|
C536780 |
|
|
silent myocardial infarction
|
3678 |
|
|
gram-negative bacterial infection
|
21678 |
|
|
emmonsia crescens infection
|
C000656784 |
|
|
basidiobolus ranarum infection
|
C000656785 |
|
|
conidiobolus coronatus infection
|
C000656785 |
|
|
gram-negative bacterial infections
|
21678 |
|
|
autosomal dominant intellectual disability 39
|
14678 |
|
|
tuberculosis of intestine
|
1678 |
|
|
endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning syndrome
|
13678 |
|
|
autosomal dominant keratoconus with early-onset anterior polar cataracts
|
13678 |
|
|
hereditary polymorphic light eruption
|
C566780 |
|
|
sensorineural hearing loss
|
20678 |
|
|
sensorineural hearing loss disorder
|
20678 |
|
