Search results for TTC8

39 hits were found for TTC8

# Family MCID Name MIFTS Score
1
P BRD002 Bardet-Biedl Syndrome 66 6.684
2
c BRD020 Bardet-Biedl Syndrome 8 48 5.489
3
c RTN106 Retinitis Pigmentosa 51 36 5.428
4
P RTN008 Retinitis Pigmentosa 77 4.939
5
P PLY006 Polydactyly 58 4.342
6
c NNS043 Nonsyndromic Retinitis Pigmentosa 27 2.774
7
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 2.725
8
P RTN018 Retinal Disease 52 2.725
9
c BRD015 Bardet-Biedl Syndrome 3 47 2.725
10
P JBR020 Joubert Syndrome 1 72 1.927
11
P LBR001 Leber Congenital Amaurosis 67 1.927
12
FND002 Fundus Dystrophy 51 1.927
13
c BRD012 Bardet-Biedl Syndrome 11 50 1.927
14
c BRD018 Bardet-Biedl Syndrome 6 48 1.927
15
c BRD032 Bardet-Biedl Syndrome 14 46 1.927
16
c BRD047 Bardet-Biedl Syndrome 16 44 1.927
17
c BRD033 Bardet-Biedl Syndrome 13 44 1.927
18
c NPH032 Nephronophthisis 4 44 1.927
19
c BRD044 Bardet-Biedl Syndrome 17 42 1.927
20
c BRD048 Bardet-Biedl Syndrome 18 40 1.927
21
c BRD045 Bardet-Biedl Syndrome 19 38 1.927
22
c BRD035 Bardet-Biedl Syndrome 15 37 1.927
23
RTN023 Retinitis 46 0.133
24
NRR001 Neuroretinitis 43 0.133
25
P RTN016 Retinal Degeneration 53 0.108
26
OBS411 Obsolete: Postaxial Polydactyly of Toes 8 0.108
27
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.077
28
c BRD010 Bardet-Biedl Syndrome 1 61 0.077
29
EYD002 Eye Disease 58 0.077
30
P PLY147 Polydactyly, Postaxial, Type A1 56 0.077
31
HYP080 Hypogonadism 50 0.077
32
ATS010 Autosomal Recessive Disease 48 0.077
33
c BRD016 Bardet-Biedl Syndrome 4 44 0.077
34
c BRD019 Bardet-Biedl Syndrome 7 42 0.077
35
P CND005 Cone Dystrophy 41 0.077
36
HYP064 Hypogonadotropism 40 0.077
37
CLP005 Ciliopathy 40 0.077
38
c RTN032 Retinal Cone Dystrophy 1 24 0.077
39
SYN149 Syndromic Rod-Cone Dystrophy 16 0.077
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