|
OMIM |
Link |
Information gain |
01 |
|
WDM
|
[NCBI]
|
0.00452947
|
|
|
MEAX
|
[NCBI]
|
0.0041494
|
|
|
myopathy, tubular aggregate
|
[NCBI]
|
0.00389461
|
|
|
myopathy with deficiency of succinate dehydrogenase and aconitase
|
[NCBI]
|
0.00317128
|
|
|
carnitine deficiency, myopathic
|
[NCBI]
|
0.00285999
|
|
|
RMD1
|
[NCBI]
|
0.00228977
|
|
|
MTM1
|
[NCBI]
|
0.00196015
|
|
|
RMD
|
[NCBI]
|
0.00179992
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
0.00172948
|
|
|
NEM3
|
[NCBI]
|
0.00172927
|
|
|
megaduodenum and/or megacystis
|
[NCBI]
|
0.00161461
|
|
|
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases
|
[NCBI]
|
0.001543
|
|
|
myopathy, distal, with onset in infancy
|
[NCBI]
|
0.00152433
|
|
|
myopathy, hyaline body, autosomal recessive
|
[NCBI]
|
0.00122532
|
|
|
MPD2
|
[NCBI]
|
0.00109085
|
|
|
myopathy, autophagic vacuolar, infantile-onset
|
[NCBI]
|
0.00109085
|
|
|
marden-walker syndrome
|
[NCBI]
|
0.00103274
|
|
|
RA
|
[NCBI]
|
0.00100233
|
|
|
CFEOM3
|
[NCBI]
|
0.000824355
|
|
|
RSMD1
|
[NCBI]
|
0.00078249
|
|
|
cardiomyopathy associated with myopathy and sudden death
|
[NCBI]
|
0.00076108
|
|
|
myopathy, congenital
|
[NCBI]
|
0.00076108
|
|
|
central core disease of muscle
|
[NCBI]
|
0.000757307
|
|
|
bethlem myopathy
|
[NCBI]
|
0.00059511
|
|
|
CF
|
[NCBI]
|
0.000572021
|
|
|
LGMD2L
|
[NCBI]
|
0.000544359
|
|
|
singleton-merten syndrome
|
[NCBI]
|
0.000544359
|
|
|
pallidopyramidal syndrome
|
[NCBI]
|
0.000544359
|
|
|
DES
|
[NCBI]
|
0.00053963
|
|
|
COL6A1
|
[NCBI]
|
0.00053855
|
|
|
BTHS
|
[NCBI]
|
0.000514838
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.000495065
|
|
|
myopathy, myosin storage
|
[NCBI]
|
0.000481686
|
|
|
minicore myopathy with external ophthalmoplegia
|
[NCBI]
|
0.000481686
|
|
|
adducted thumbs syndrome
|
[NCBI]
|
0.00046333
|
|
|
CAV3
|
[NCBI]
|
0.000453367
|
|
|
glycogen storage disease ii
|
[NCBI]
|
0.000426128
|
|
|
mitochondrial myopathy
|
[NCBI]
|
0.00042468
|
|
|
myopathy, centronuclear, autosomal dominant
|
[NCBI]
|
0.00042468
|
|
|
MEHMO
|
[NCBI]
|
0.000411145
|
|
|
SLE
|
[NCBI]
|
0.000399834
|
|
|
MHS1
|
[NCBI]
|
0.000393386
|
|
|
GSM1
|
[NCBI]
|
0.000372658
|
|
|
KSS
|
[NCBI]
|
0.000371454
|
|
|
visceral myopathy, familial, with external ophthalmoplegia
|
[NCBI]
|
0.000342239
|
|
|
HMERF
|
[NCBI]
|
0.000331488
|
|
|
alpha-b crystallinopathy
|
[NCBI]
|
0.000331488
|
|
|
HMN7A
|
[NCBI]
|
0.000317152
|
|
|
inclusion body myositis
|
[NCBI]
|
0.000317152
|
|
|
RYR1
|
[NCBI]
|
0.000314284
|
|
|
glycogen storage disease vii
|
[NCBI]
|
0.000302802
|
|
|
cataract and cardiomyopathy
|
[NCBI]
|
0.000295853
|
|
|
MTM1
|
[NCBI]
|
0.000293417
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
0.000280383
|
|
|
AMPD1
|
[NCBI]
|
0.000277695
|
|
|
muscle glycogenosis, x-linked
|
[NCBI]
|
0.000269773
|
|
|
native american myopathy
|
[NCBI]
|
0.000269773
|
|
|
MELAS
|
[NCBI]
|
0.000267609
|
|
|
CRYAB
|
[NCBI]
|
0.000258106
|
|
|
myopathy, centronuclear, autosomal recessive
|
[NCBI]
|
0.000254288
|
|
|
MTTL1
|
[NCBI]
|
0.000252276
|
|
|
myopathy with giant abnormal mitochondria
|
[NCBI]
|
0.000248571
|
|
|
tibial muscular dystrophy, tardive
|
[NCBI]
|
0.000243299
|
|
|
CDSP
|
[NCBI]
|
0.000243294
|
|
|
MYH7
|
[NCBI]
|
0.000243199
|
|
|
mitochondrial myopathy with diabetes
|
[NCBI]
|
0.000241987
|
|
|
COL6A2
|
[NCBI]
|
0.000237952
|
|
|
glycogen storage disease v
|
[NCBI]
|
0.000237389
|
|
|
danon disease
|
[NCBI]
|
0.00023358
|
|
|
brody myopathy
|
[NCBI]
|
0.000222974
|
|
|
skin creases, multiple benign ring-shaped, of limbs
|
[NCBI]
|
0.000221664
|
|
|
TAZ
|
[NCBI]
|
0.000213348
|
|
|
megacystis-microcolon-intestinal hypoperistalsis syndrome
|
[NCBI]
|
0.000210798
|
|
|
ATP2A1
|
[NCBI]
|
0.000207532
|
|
|
EKD1
|
[NCBI]
|
0.000193669
|
|
|
COL6A3
|
[NCBI]
|
0.000193624
|
|
|
ACHE
|
[NCBI]
|
0.000187809
|
|
|
mitochondrial complex iii deficiency
|
[NCBI]
|
0.000181446
|
|
|
MM
|
[NCBI]
|
0.000175634
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1
|
[NCBI]
|
0.000174437
|
|
|
CACNA1S
|
[NCBI]
|
0.00016871
|
|
|
pleoconial myopathy with salt craving
|
[NCBI]
|
0.000165684
|
|
|
minicore myopathy, antenatal onset, with arthrogryposis
|
[NCBI]
|
0.000165684
|
|
|
MNGIE
|
[NCBI]
|
0.00016415
|
|
|
HYPP
|
[NCBI]
|
0.000163866
|
|
|
IBM3
|
[NCBI]
|
0.000163265
|
|
|
growth-mental deficiency syndrome of myhre
|
[NCBI]
|
0.00015023
|
|
|
LGMD2H
|
[NCBI]
|
0.00015023
|
|
|
acyl-coa dehydrogenase, short-chain, deficiency of
|
[NCBI]
|
0.00015023
|
|
|
TRIM32
|
[NCBI]
|
0.000143735
|
|
|
PHKA1
|
[NCBI]
|
0.000143735
|
|
|
glycogen storage disease iv
|
[NCBI]
|
0.00014306
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
0.000140878
|
|
|
MSS
|
[NCBI]
|
0.000138774
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive
|
[NCBI]
|
0.000135707
|
|
|
myopathy, spheroid body
|
[NCBI]
|
0.000134827
|
|
|
myopathy with storage of glycoproteins and glycosaminoglycans
|
[NCBI]
|
0.000134827
|
|
|
MTTK
|
[NCBI]
|
0.000134315
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
0.000131038
|
|
|
CFTD
|
[NCBI]
|
0.000121519
|
|
|
coffin-siris syndrome
|
[NCBI]
|
0.000120868
|
|
|
FMF
|
[NCBI]
|
0.000112366
|
|
|
IBM2
|
[NCBI]
|
0.000110717
|
|
|
udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase
|
[NCBI]
|
0.00010907
|
|
|
TTN
|
[NCBI]
|
0.000107426
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
0.000106156
|
|
|
XK
|
[NCBI]
|
0.000104391
|
|
|
LGMD1C
|
[NCBI]
|
9.82852e-05
|
|
|
RCM1
|
[NCBI]
|
9.33449e-05
|
|
|
MPD1
|
[NCBI]
|
9.33449e-05
|
|
|
poland syndrome
|
[NCBI]
|
9.27095e-05
|
|
|
TK2
|
[NCBI]
|
8.95192e-05
|
|
|
ETFDH
|
[NCBI]
|
8.95192e-05
|
|
|
SEPN1
|
[NCBI]
|
8.58694e-05
|
|
|
phosphoglycerate mutase, muscle, deficiency of
|
[NCBI]
|
8.58694e-05
|
|
|
glycogen storage disease iii
|
[NCBI]
|
8.57382e-05
|
|
|
trismus-pseudocamptodactyly syndrome
|
[NCBI]
|
8.53489e-05
|
|
|
myopathy, congenital, with crystalline intranuclear inclusions
|
[NCBI]
|
8.28268e-05
|
|
|
neurologic disease, infantile multisystem, with osseous fragility
|
[NCBI]
|
8.28268e-05
|
|
|
camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia
|
[NCBI]
|
8.28268e-05
|
|
|
ataxia with fasciculations
|
[NCBI]
|
8.28268e-05
|
|
|
hypermetabolism due to defect in mitochondria
|
[NCBI]
|
8.28268e-05
|
|
|
myopathy due to malate-aspartate shuttle defect
|
[NCBI]
|
8.28268e-05
|
|
|
dystonia with ringbinden
|
[NCBI]
|
8.28268e-05
|
|
|
NLSDM
|
[NCBI]
|
8.28268e-05
|
|
|
XMPMA
|
[NCBI]
|
8.28268e-05
|
|
|
muscular dystrophy, cardiac type
|
[NCBI]
|
8.28268e-05
|
|
|
muscular hypoplasia, congenital universal, of krabbe
|
[NCBI]
|
8.28268e-05
|
|
|
amyotrophic dystonic paraplegia
|
[NCBI]
|
8.28268e-05
|
|
|
myotilinopathy
|
[NCBI]
|
8.28268e-05
|
|
|
stormorken syndrome
|
[NCBI]
|
8.28268e-05
|
|
|
fingerprint body myopathy
|
[NCBI]
|
8.28268e-05
|
|
|
gamstorp-wohlfart syndrome
|
[NCBI]
|
8.28268e-05
|
|
|
mitochondrial myopathy with a defect in mitochondrial-protein transport
|
[NCBI]
|
8.28268e-05
|
|
|
encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts
|
[NCBI]
|
8.28268e-05
|
|
|
myopathy with abnormal lipid metabolism
|
[NCBI]
|
8.28268e-05
|
|
|
TTID
|
[NCBI]
|
8.27962e-05
|
|
|
TNF
|
[NCBI]
|
8.07134e-05
|
|
|
parkinson disease, mitochondrial
|
[NCBI]
|
7.90166e-05
|
|
|
MERRF
|
[NCBI]
|
7.62864e-05
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
7.42657e-05
|
|
|
mitochondrial dna depletion syndrome, myopathic form
|
[NCBI]
|
7.37836e-05
|
|
|
phosphoglycerate kinase 1 deficiency
|
[NCBI]
|
7.37836e-05
|
|
|
NM
|
[NCBI]
|
7.37836e-05
|
|
|
DWS
|
[NCBI]
|
7.15787e-05
|
|
|
CDS
|
[NCBI]
|
7.14745e-05
|
|
|
CFEOM1
|
[NCBI]
|
7.14745e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
7.14159e-05
|
|
|
coenzyme q10 deficiency
|
[NCBI]
|
6.9332e-05
|
|
|
EDMD
|
[NCBI]
|
6.74317e-05
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
6.73347e-05
|
|
|
APC
|
[NCBI]
|
6.70397e-05
|
|
|
AHDS
|
[NCBI]
|
6.54647e-05
|
|
|
mulibrey nanism
|
[NCBI]
|
6.54647e-05
|
|
|
ENO3
|
[NCBI]
|
6.36884e-05
|
|
|
MYF6
|
[NCBI]
|
6.36884e-05
|
|
|
MYOG
|
[NCBI]
|
6.36884e-05
|
|
|
AMPD3
|
[NCBI]
|
6.36884e-05
|
|
|
MTCYB
|
[NCBI]
|
6.3081e-05
|
|
|
MSTN
|
[NCBI]
|
6.20766e-05
|
|
|
BRRS
|
[NCBI]
|
6.10608e-05
|
|
|
myotonia congenita, autosomal dominant
|
[NCBI]
|
6.04843e-05
|
|
|
CMH10
|
[NCBI]
|
6.04523e-05
|
|
|
mental retardation, x-linked, with short stature, small testes, muscle wasting, and tremor
|
[NCBI]
|
6.04523e-05
|
|
|
mitochondrial myopathy with lactic acidosis
|
[NCBI]
|
6.04523e-05
|
|
|
erythrocyte lactate transporter defect
|
[NCBI]
|
6.04523e-05
|
|
|
CMH8
|
[NCBI]
|
6.04523e-05
|
|
|
CDG2D
|
[NCBI]
|
6.04523e-05
|
|
|
spinal muscular atrophy, scapuloperoneal
|
[NCBI]
|
6.04523e-05
|
|
|
filaminopathy, autosomal dominant
|
[NCBI]
|
6.04523e-05
|
|
|
anal sphincter myopathy, internal
|
[NCBI]
|
6.04523e-05
|
|
|
LMNA
|
[NCBI]
|
6.02957e-05
|
|
|
PMC
|
[NCBI]
|
5.75877e-05
|
|
|
UCMD
|
[NCBI]
|
5.62436e-05
|
|
|
DYSF
|
[NCBI]
|
5.4174e-05
|
|
|
MADA
|
[NCBI]
|
5.37346e-05
|
|
|
MB
|
[NCBI]
|
5.31686e-05
|
|
|
HOKPP
|
[NCBI]
|
5.25603e-05
|
|
|
myotubular myopathy with abnormal genital development
|
[NCBI]
|
5.20682e-05
|
|
|
crisponi syndrome
|
[NCBI]
|
5.20682e-05
|
|
|
alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus
|
[NCBI]
|
5.20682e-05
|
|
|
neuropathy, ataxia, and retinitis pigmentosa
|
[NCBI]
|
5.20682e-05
|
|
|
myopathy, congenital nonprogressive, with moebius sequence and robin sequence
|
[NCBI]
|
5.20682e-05
|
|
|
LIMM
|
[NCBI]
|
5.20682e-05
|
|
|
EXOSC10
|
[NCBI]
|
4.99241e-05
|
|
|
MYH2
|
[NCBI]
|
4.99241e-05
|
|
|
MTMR3
|
[NCBI]
|
4.99241e-05
|
|
|
NBR1
|
[NCBI]
|
4.99241e-05
|
|
|
MYL3
|
[NCBI]
|
4.99241e-05
|
|
|
POLG
|
[NCBI]
|
4.96034e-05
|
|
|
VCP
|
[NCBI]
|
4.91031e-05
|
|
|
CHNG2
|
[NCBI]
|
4.83106e-05
|
|
|
MADD
|
[NCBI]
|
4.73451e-05
|
|
|
retinitis pigmentosa-deafness syndrome
|
[NCBI]
|
4.6658e-05
|
|
|
corticosteroid-binding globulin deficiency
|
[NCBI]
|
4.6658e-05
|
|
|
satoyoshi syndrome
|
[NCBI]
|
4.6658e-05
|
|
|
HRAS
|
[NCBI]
|
4.55234e-05
|
|
|
COL15A1
|
[NCBI]
|
4.4739e-05
|
|
|
FHL1
|
[NCBI]
|
4.4739e-05
|
|
|
FLNC
|
[NCBI]
|
4.4739e-05
|
|
|
KY
|
[NCBI]
|
4.4739e-05
|
|
|
LMO7
|
[NCBI]
|
4.4739e-05
|
|
|
UCHL3
|
[NCBI]
|
4.4739e-05
|
|
|
MTTV
|
[NCBI]
|
4.4739e-05
|
|
|
SOX6
|
[NCBI]
|
4.4739e-05
|
|
|
MLASA
|
[NCBI]
|
4.26602e-05
|
|
|
EDM3
|
[NCBI]
|
4.26602e-05
|
|
|
PGAM1
|
[NCBI]
|
4.13775e-05
|
|
|
ITGA7
|
[NCBI]
|
4.13775e-05
|
|
|
PHKB
|
[NCBI]
|
4.13775e-05
|
|
|
CXORF6
|
[NCBI]
|
4.13775e-05
|
|
|
ETFB
|
[NCBI]
|
4.13775e-05
|
|
|
CUL4B
|
[NCBI]
|
4.13775e-05
|
|
|
PD
|
[NCBI]
|
4.08186e-05
|
|
|
fumarase deficiency
|
[NCBI]
|
3.94942e-05
|
|
|
phosphorylase kinase deficiency of liver and muscle, autosomal recessive
|
[NCBI]
|
3.94942e-05
|
|
|
MAP4
|
[NCBI]
|
3.88822e-05
|
|
|
BIN1
|
[NCBI]
|
3.88822e-05
|
|
|
MYL2
|
[NCBI]
|
3.88822e-05
|
|
|
MTMR1
|
[NCBI]
|
3.88822e-05
|
|
|
COL9A3
|
[NCBI]
|
3.6897e-05
|
|
|
MTND2
|
[NCBI]
|
3.6897e-05
|
|
|
XBP1
|
[NCBI]
|
3.6897e-05
|
|
|
MTTH
|
[NCBI]
|
3.6897e-05
|
|
|
EAD
|
[NCBI]
|
3.68779e-05
|
|
|
SPMM
|
[NCBI]
|
3.68779e-05
|
|
|
optic atrophy 1 and deafness
|
[NCBI]
|
3.68779e-05
|
|
|
mitochondrial complex ii deficiency
|
[NCBI]
|
3.68779e-05
|
|
|
SJS1
|
[NCBI]
|
3.66312e-05
|
|
|
PTH
|
[NCBI]
|
3.56369e-05
|
|
|
SIL1
|
[NCBI]
|
3.52488e-05
|
|
|
SLN
|
[NCBI]
|
3.52488e-05
|
|
|
ACTG1
|
[NCBI]
|
3.52488e-05
|
|
|
CRLF1
|
[NCBI]
|
3.52488e-05
|
|
|
aging
|
[NCBI]
|
3.46523e-05
|
|
|
carnitine palmitoyltransferase i deficiency
|
[NCBI]
|
3.46523e-05
|
|
|
CMRD
|
[NCBI]
|
3.46523e-05
|
|
|
lactic acidosis, fatal infantile
|
[NCBI]
|
3.46523e-05
|
|
|
IBMPFD
|
[NCBI]
|
3.46523e-05
|
|
|
LSFC
|
[NCBI]
|
3.46523e-05
|
|
|
MEG3
|
[NCBI]
|
3.38402e-05
|
|
|
SDHC
|
[NCBI]
|
3.38402e-05
|
|
|
UBB
|
[NCBI]
|
3.38402e-05
|
|
|
ACADM
|
[NCBI]
|
3.37222e-05
|
|
|
DM2
|
[NCBI]
|
3.26289e-05
|
|
|
CACNA1C
|
[NCBI]
|
3.26108e-05
|
|
|
costello syndrome
|
[NCBI]
|
3.21092e-05
|
|
|
ACTA1
|
[NCBI]
|
3.15203e-05
|
|
|
GBE1
|
[NCBI]
|
3.15203e-05
|
|
|
LAMP2
|
[NCBI]
|
3.15203e-05
|
|
|
GARS
|
[NCBI]
|
3.0541e-05
|
|
|
PNPLA2
|
[NCBI]
|
3.0541e-05
|
|
|
MTMR2
|
[NCBI]
|
3.0541e-05
|
|
|
PFKM
|
[NCBI]
|
2.96524e-05
|
|
|
LDHA
|
[NCBI]
|
2.96524e-05
|
|
|
SPG17
|
[NCBI]
|
2.94863e-05
|
|
|
hyperlysinemia
|
[NCBI]
|
2.94863e-05
|
|
|
CPT2
|
[NCBI]
|
2.88394e-05
|
|
|
NEB
|
[NCBI]
|
2.88394e-05
|
|
|
OPMD
|
[NCBI]
|
2.85382e-05
|
|
|
schwannomatosis
|
[NCBI]
|
2.81087e-05
|
|
|
trifunctional protein deficiency
|
[NCBI]
|
2.81087e-05
|
|
|
lipomatosis, familial benign cervical
|
[NCBI]
|
2.81087e-05
|
|
|
MTCO2
|
[NCBI]
|
2.80904e-05
|
|
|
LAMA2
|
[NCBI]
|
2.80904e-05
|
|
|
ACADVL
|
[NCBI]
|
2.80904e-05
|
|
|
RP
|
[NCBI]
|
2.78495e-05
|
|
|
HADHA
|
[NCBI]
|
2.73961e-05
|
|
|
CD
|
[NCBI]
|
2.71756e-05
|
|
|
congenital cataracts, facial dysmorphism, and neuropathy
|
[NCBI]
|
2.68544e-05
|
|
|
methionine adenosyltransferase deficiency
|
[NCBI]
|
2.68544e-05
|
|
|
SLC16A1
|
[NCBI]
|
2.55753e-05
|
|
|
NR4A3
|
[NCBI]
|
2.55753e-05
|
|
|
SLC22A5
|
[NCBI]
|
2.50391e-05
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
2.46435e-05
|
|
|
LGMD2B
|
[NCBI]
|
2.46435e-05
|
|
|
PYGM
|
[NCBI]
|
2.40512e-05
|
|
|
xanthinuria, type i
|
[NCBI]
|
2.36602e-05
|
|
|
EA1
|
[NCBI]
|
2.36602e-05
|
|
|
OPA1
|
[NCBI]
|
2.35941e-05
|
|
|
SLC25A4
|
[NCBI]
|
2.35941e-05
|
|
|
acyl-coa dehydrogenase, very long-chain, deficiency of
|
[NCBI]
|
2.27445e-05
|
|
|
ACADS
|
[NCBI]
|
2.27425e-05
|
|
|
FTD
|
[NCBI]
|
2.24026e-05
|
|
|
SCCMS
|
[NCBI]
|
2.18885e-05
|
|
|
septooptic dysplasia
|
[NCBI]
|
2.18885e-05
|
|
|
RYR2
|
[NCBI]
|
2.12453e-05
|
|
|
MTND1
|
[NCBI]
|
2.12453e-05
|
|
|
VED
|
[NCBI]
|
2.10856e-05
|
|
|
oca2 gene
|
[NCBI]
|
2.09066e-05
|
|
|
PLN
|
[NCBI]
|
2.05801e-05
|
|
|
CAPN3
|
[NCBI]
|
2.05801e-05
|
|
|
DMD
|
[NCBI]
|
1.99971e-05
|
|
|
fucosidosis
|
[NCBI]
|
1.99608e-05
|
|
|
PRL
|
[NCBI]
|
1.99491e-05
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
1.96665e-05
|
|
|
XPA
|
[NCBI]
|
1.93816e-05
|
|
|
EDMD2
|
[NCBI]
|
1.89433e-05
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
1.89433e-05
|
|
|
MDC1A
|
[NCBI]
|
1.83043e-05
|
|
|
GSD
|
[NCBI]
|
1.83043e-05
|
|
|
NBIA1
|
[NCBI]
|
1.83043e-05
|
|
|
hyperekplexia, hereditary
|
[NCBI]
|
1.83043e-05
|
|
|
SCN4A
|
[NCBI]
|
1.7842e-05
|
|
|
MTATP6
|
[NCBI]
|
1.7842e-05
|
|
|
HNA
|
[NCBI]
|
1.76974e-05
|
|
|
DMD
|
[NCBI]
|
1.75292e-05
|
|
|
GAN1
|
[NCBI]
|
1.71199e-05
|
|
|
DMPK
|
[NCBI]
|
1.63348e-05
|
|
|
BCL2
|
[NCBI]
|
1.57625e-05
|
|
|
hyperglycerolemia
|
[NCBI]
|
1.55416e-05
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
1.55416e-05
|
|
|
SCN5A
|
[NCBI]
|
1.54015e-05
|
|
|
APOA1
|
[NCBI]
|
1.54015e-05
|
|
|
CGL2
|
[NCBI]
|
1.50606e-05
|
|
|
PDB
|
[NCBI]
|
1.50606e-05
|
|
|
MTND4
|
[NCBI]
|
1.48878e-05
|
|
|
EPO
|
[NCBI]
|
1.42793e-05
|
|
|
HFTC
|
[NCBI]
|
1.41574e-05
|
|
|
LGMD2C
|
[NCBI]
|
1.3324e-05
|
|
|
PNKD1
|
[NCBI]
|
1.3324e-05
|
|
|
EFE
|
[NCBI]
|
1.3324e-05
|
|
|
LBP
|
[NCBI]
|
1.32405e-05
|
|
|
FPLD2
|
[NCBI]
|
1.29308e-05
|
|
|
DA2A
|
[NCBI]
|
1.25521e-05
|
|
|
ZS
|
[NCBI]
|
1.23538e-05
|
|
|
SMA3
|
[NCBI]
|
1.2187e-05
|
|
|
CHAC
|
[NCBI]
|
1.18348e-05
|
|
|
MEB
|
[NCBI]
|
1.14948e-05
|
|
|
OCA2
|
[NCBI]
|
1.11663e-05
|
|
|
COH1
|
[NCBI]
|
9.95651e-06
|
|
|
campomelic dysplasia
|
[NCBI]
|
9.95651e-06
|
|
|
CMD1A
|
[NCBI]
|
9.67765e-06
|
|
|
XPA
|
[NCBI]
|
9.40735e-06
|
|
|
SERPINA6
|
[NCBI]
|
9.39539e-06
|
|
|
BMD
|
[NCBI]
|
8.89098e-06
|
|
|
MAPT
|
[NCBI]
|
8.70632e-06
|
|
|
CMH
|
[NCBI]
|
7.77084e-06
|
|
|
CLN3
|
[NCBI]
|
7.72616e-06
|
|
|
DYT1
|
[NCBI]
|
7.51257e-06
|
|
|
CTNS
|
[NCBI]
|
7.30486e-06
|
|
|
DCK
|
[NCBI]
|
7.16194e-06
|
|
|
RSTS
|
[NCBI]
|
5.83115e-06
|
|
|
PMP22
|
[NCBI]
|
5.57922e-06
|
|
|
NF2
|
[NCBI]
|
5.50872e-06
|
|
|
CLS
|
[NCBI]
|
5.3536e-06
|
|
|
NGFB
|
[NCBI]
|
5.20831e-06
|
|
|
MPO
|
[NCBI]
|
4.91786e-06
|
|
|
PRNP
|
[NCBI]
|
4.29988e-06
|
|
|
NPC1
|
[NCBI]
|
3.99893e-06
|
|
|
HGPS
|
[NCBI]
|
3.88097e-06
|
|
|
FOP
|
[NCBI]
|
3.65353e-06
|
|
|
WRN
|
[NCBI]
|
3.54389e-06
|
|
|
PWS
|
[NCBI]
|
2.77449e-06
|
|
|
CAT
|
[NCBI]
|
2.58701e-06
|
|
|
LS
|
[NCBI]
|
2.2584e-06
|
|
|
MUC1
|
[NCBI]
|
1.9837e-06
|
|
|
NF1
|
[NCBI]
|
1.56788e-06
|
|
|
G6PD
|
[NCBI]
|
1.50892e-06
|
|
|
SMS
|
[NCBI]
|
1.40351e-06
|
|
|
CDLS1
|
[NCBI]
|
8.76291e-07
|
|
|
FRAP1
|
[NCBI]
|
8.25605e-07
|
|
|
HGF
|
[NCBI]
|
5.91694e-07
|
|
|
WBS
|
[NCBI]
|
2.97005e-07
|
|
|
MG
|
[NCBI]
|
1.30877e-07
|
|
|
SMAX1
|
[NCBI]
|
1.22305e-07
|
|
|
HD
|
[NCBI]
|
3.27806e-08
|
|
|
APOB
|
[NCBI]
|
2.25466e-08
|
|
|
TTR
|
[NCBI]
|
7.89102e-09
|
|
|
LPL
|
[NCBI]
|
1.06559e-09
|
|