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Hypogonadotropic hypogonadism 1 with or without anosmia (HH1)
|
ANOS1
|
XL
|
1
|
1
|
2
|
2
|
0
|
0
|
Hypogonadotropic hypogonadism 1 with or without anosmia (HH1)
|
KAL1
|
XL
|
1
|
2
|
1
|
1
|
1
|
1
|
Hypoparathyroidism–retardation–dysmorphism syndrome (HRDS)
|
TBCE
|
1R
|
1
|
1
|
1
|
2
|
0
|
0
|
Hypophosphatasia, infantile
|
ALPL
|
AR
|
6
|
7
|
6
|
9
|
4
|
4
|
Ichthyosis, congenital, autosomal recessive 1 (ARCI1)
|
TGM1
|
AD
|
2
|
9
|
7
|
10
|
1
|
1
|
Ichthyosis, lamellar, 2 (LI2)
|
ABCA12
|
AR
|
2
|
2
|
1
|
2
|
0
|
0
|
Ichthyosis, spastic quadriplegia, and mental retardation (ISQMR)
|
ELOVL4
|
AR
|
1
|
1
|
1
|
1
|
0
|
0
|
Ichthyosis, X‐linked (XLI)
|
STS
|
XL
|
2
|
3
|
3
|
4
|
1
|
1
|
Ifap syndrome with or without Bresheck syndrome
|
MBTPS2
|
XL
|
2
|
3
|
2
|
5
|
2
|
1
|
Immunodeficiency with hyper‐IgM, type 1 (HIGM1)
|
CD40LG
|
XL
|
4
|
14
|
14
|
22
|
6
|
6
|
Immunodysregulation, polyendocrinopathy, and enteropathy, X‐linked (IPEX)
|
FOXP3
|
XL
|
2
|
3
|
3
|
3
|
1
|
1
|
Incontinentia pigmenti (IP)
|
IKBKG
|
XL
|
15
|
35
|
28
|
43
|
11
|
11
|
Infantile cerebellar‐retinal degeneration (ICRD)
|
ACO2
|
AR
|
1
|
1
|
1
|
2
|
2
|
2
|
Infantile liver failure syndrome 1 (ILFS1)
|
LARS
|
AR
|
1
|
1
|
2
|
2
|
1
|
1
|
Isovaleric acidemia (IVA)
|
IVD
|
AR
|
1
|
1
|
1
|
2
|
0
|
0
|
Joubert syndrome 1 (JBTS1)
|
INPP5E
|
AR
|
1
|
1
|
2
|
2
|
1
|
1
|
Joubert syndrome 17 (JBTS17)
|
CPLANE1
|
AD
|
1
|
1
|
1
|
2
|
1
|
1
|
Joubert syndrome 2 (JBTS2)
|
TMEM216
|
AR
|
1
|
1
|
2
|
2
|
1
|
1
|
Joubert syndrome 21 (JBTS21)
|
CSPP1
|
AR
|
2
|
5
|
4
|
7
|
1
|
1
|
Joubert syndrome 23 (JBTS23)
|
KIAA0586
|
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