|
SLC25A23
|
608746 |
|
|
glycogen storage disease 10
|
261670 |
|
|
Glycogen storage disease
|
PS232200 |
|
|
oeis complex
|
258040 |
|
|
pseudopapilledema
|
177800 |
|
|
C1QTNF5
|
608752 |
|
|
cardiomyopathy, familial hypertrophic, 8
|
608751 |
|
|
ALG3
|
608750 |
|
|
SLC2A5
|
138230 |
|
|
TSEN15
|
608756 |
|
|
TSEN54
|
608755 |
|
|
TSEN34
|
608754 |
|
|
TSEN2
|
608753 |
|
|
Three M syndrome
|
PS273750 |
|
|
deafness, autosomal dominant 74
|
618140 |
|
|
microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome
|
618142 |
|
|
developmental and epileptic encephalopathy 67
|
618141 |
|
|
usher syndrome, type 4
|
618144 |
|
|
Usher syndrome
|
PS276900 |
|
|
developmental and epileptic encephalopathy 95
|
618143 |
|
