|
athabaskan severe combined immunodeficiency
|
C536786 |
|
|
t-cell immunodeficiency, congenital alopecia, and nail dystrophy
|
C536781 |
|
|
KCNV2-Related cone dystrophy with night blindness and supernormal rod responses
|
C563678 |
|
|
silent myocardial infarction
|
3678 |
|
|
endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome
|
13678 |
|
|
endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning syndrome
|
13678 |
|
|
primary t-cell immunodeficiency disorders
|
C536780 |
|
|
t cell immunodeficiency primary
|
C536780 |
|
|
autosomal dominant keratoconus with early-onset anterior polar cataracts
|
13678 |
|
|
spastic ataxia of charlevoix-saguenay
|
C536787 |
|
|
charlevoix-saguenay type spastic ataxia
|
C536787 |
|
|
autosomal recessive spastic ataxia 6
|
C536787 |
|
|
autosomal recessive spastic ataxia of charlevoix-saguenay
|
C536787 |
|
