Search results for arl13b

54 hits were found for arl13b

# Family MCID Name MIFTS Score
1
c JBR013 Joubert Syndrome 8 42 5.426
2
P JBR020 Joubert Syndrome 1 72 4.583
3
P BRD002 Bardet-Biedl Syndrome 66 2.470
4
P MCK013 Meckel Syndrome, Type 1 65 2.470
5
P MDL005 Medulloblastoma 77 2.432
6
ALK013 Alkaptonuria 58 2.432
7
P NPH005 Nephronophthisis 58 2.432
8
P RTN008 Retinitis Pigmentosa 77 1.746
9
P LBR001 Leber Congenital Amaurosis 67 1.746
10
P VSC013 Visceral Heterotaxy 52 1.746
11
P PRM011 Primary Ciliary Dyskinesia 69 1.688
12
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 63 1.688
13
P CRN108 Cranioectodermal Dysplasia 1 62 1.688
14
ELL001 Ellis-Van Creveld Syndrome 62 1.688
15
P SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 60 1.688
16
P SNR003 Senior-Loken Syndrome 1 57 1.688
17
c CRP023 Carpenter Syndrome 1 56 1.688
18
P HYD033 Hydrolethalus Syndrome 1 56 1.688
19
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 55 1.688
20
P CYS039 Cystic Kidney Disease 54 1.688
21
CLB010 Coloboma of Macula 53 1.688
22
c ORF034 Orofaciodigital Syndrome Vi 52 1.688
23
c JBR041 Joubert Syndrome 3 52 1.688
24
FND002 Fundus Dystrophy 51 1.688
25
KRT010 Kartagener Syndrome 50 1.688
26
c MCK032 Meckel Syndrome, Type 3 49 1.688
27
c JBR018 Joubert Syndrome 4 49 1.688
28
P ORF001 Orofaciodigital Syndrome 48 1.688
29
c JBR004 Joubert Syndrome 2 47 1.688
30
c MCK033 Meckel Syndrome, Type 4 46 1.688
31
c JBR011 Joubert Syndrome 7 45 1.688
32
c JBR015 Joubert Syndrome 6 45 1.688
33
c JBR035 Joubert Syndrome 24 43 1.688
34
c JBR016 Joubert Syndrome 10 43 1.688
35
c RTN162 Retinitis Pigmentosa 2 43 1.688
36
PHY002 Physical Disorder 42 1.688
37
c JBR014 Joubert Syndrome 9 42 1.688
38
ASP005 Asphyxiating Thoracic Dystrophy 42 1.688
39
c JBR031 Joubert Syndrome 21 41 1.688
40
END059 Endocrine-Cerebroosteodysplasia 39 1.688
41
CLP005 Ciliopathy 40 0.201
42
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.142
43
P RTN016 Retinal Degeneration 53 0.123
44
P LNG028 Long Qt Syndrome 65 0.101
45
ACR006 Aceruloplasminemia 73 0.071
46
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.071
47
P ART023 Arthropathy 62 0.071
48
P SCL018 Scoliosis 60 0.071
49
P PLY006 Polydactyly 58 0.071
50
APR001 Apraxia 51 0.071
51
RTN023 Retinitis 46 0.071
52
NRR001 Neuroretinitis 43 0.071
53
P HYP265 Hypotonia 42 0.071
54
OCL015 Oculomotor Apraxia 35 0.071
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