|
leukodystrophy, hypomyelinating, 17
|
618006 |
|
|
Leukodystrophy, hypomyelinating
|
PS312080 |
|
|
pseudohypoaldosteronism, type i, autosomal dominant
|
177735 |
|
|
Pseudohypoaldosteronism, type I
|
PS177735 |
|
|
ADM2
|
608682 |
|
|
CHR_9606chr5q31.1
|
CHR_9606chr5q31.1 |
|
|
spondylocostal dysostosis 2, autosomal recessive
|
608681 |
|
|
Spondylocostal dysostosis
|
PS277300 |
|
|
OIP5
|
606020 |
|
|
TPRKB
|
608680 |
|
|
CHR_9606chr5q31.3
|
CHR_9606chr5q31.3 |
|
|
leopard syndrome 1
|
151100 |
|
|
LEOPARD syndrome
|
PS151100 |
|
|
CHR_9606chr5q31.2
|
CHR_9606chr5q31.2 |
|
|
POLR2H
|
606023 |
|
|
RAB3IP
|
608686 |
|
|
SMC1B
|
608685 |
|
|
606024
|
606024 |
|
|
SLC2A1
|
138140 |
|
|
NIN
|
608684 |
|
