|
mitochondrial complex V (ATP synthase) deficiency
|
14471 |
|
|
congenital melanocytic Nevus
|
44792 |
|
|
congenital melanocytic Nevus of skin
|
44792 |
|
|
congenital pigmented Nevus of skin
|
44792 |
|
|
congenital melanocytic Nevus of the skin
|
44792 |
|
|
congenital pigmented Nevus of the skin
|
44792 |
|
|
RPS6KA3 non-syndromic X-linked intellectual disability
|
10447 |
|
|
intellectual disability, X-linked type 19
|
10447 |
|
|
mental retardation, X-linked type 19
|
10447 |
|
|
infantile periodic alternating nystagmus 5
|
C564478 |
|
|
sleep related abnormal swallowing syndrome
|
D020447 |
|
|
Gabriele de Vries syndrome
|
44738 |
|
