Search results for ift88

51 hits were found for ift88

# Family MCID Name MIFTS Score
1
P KDN018 Kidney Disease 72 3.786
2
P PLY014 Polycystic Kidney Disease 62 3.393
3
P RTN008 Retinitis Pigmentosa 79 2.948
4
CLF027 Cleft Palate, Isolated 64 2.493
5
P RTN016 Retinal Degeneration 53 2.493
6
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 2.421
7
P JBR020 Joubert Syndrome 1 72 2.375
8
P MCK013 Meckel Syndrome, Type 1 65 2.375
9
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 2.375
10
P MCR010 Microcephaly 59 2.375
11
c SHR072 Short-Rib Thoracic Dysplasia 3 with or Without Polydactyly 58 2.375
12
P CYS039 Cystic Kidney Disease 54 2.375
13
P PRM011 Primary Ciliary Dyskinesia 69 1.680
14
LBR036 Leber Plus Disease 66 1.680
15
P BRD002 Bardet-Biedl Syndrome 66 1.680
16
ELL001 Ellis-Van Creveld Syndrome 62 1.680
17
c BRD010 Bardet-Biedl Syndrome 1 62 1.680
18
P CRN108 Cranioectodermal Dysplasia 1 62 1.680
19
c ORF037 Orofaciodigital Syndrome I 60 1.680
20
P NPH005 Nephronophthisis 59 1.680
21
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 57 1.680
22
P SNR003 Senior-Loken Syndrome 1 56 1.680
23
FND002 Fundus Dystrophy 55 1.680
24
c SHR075 Short-Rib Thoracic Dysplasia 9 with or Without Polydactyly 53 1.680
25
P VSC013 Visceral Heterotaxy 52 1.680
26
c NPH030 Nephronophthisis 2 50 1.680
27
c BRD020 Bardet-Biedl Syndrome 8 50 1.680
28
KRT010 Kartagener Syndrome 50 1.680
29
c MCK032 Meckel Syndrome, Type 3 50 1.680
30
c BRD018 Bardet-Biedl Syndrome 6 49 1.680
31
c BRD015 Bardet-Biedl Syndrome 3 48 1.680
32
P ORF001 Orofaciodigital Syndrome 48 1.680
33
c PRM031 Primary Autosomal Recessive Microcephaly 47 1.680
34
c JBR035 Joubert Syndrome 24 46 1.680
35
c SPN305 Spinocerebellar Ataxia 11 45 1.680
36
ASP005 Asphyxiating Thoracic Dystrophy 43 1.680
37
PHY002 Physical Disorder 42 1.680
38
CRB033 Cerebral Degeneration 42 1.680
39
c CLR136 Ciliary Dyskinesia, Primary, 9 41 1.680
40
c SMP005 Simpson-Golabi-Behmel Syndrome, Type 2 40 1.680
41
CLP005 Ciliopathy 43 0.176
42
P SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 60 0.102
43
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.102
44
CLF001 Cleft Lip 53 0.102
45
CYS001 Cystic Fibrosis 81 0.072
46
P PLM036 Pulmonary Fibrosis 65 0.072
47
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.072
48
THY029 Thyroid Carcinoma 59 0.072
49
CLF004 Cleft Lip/palate 54 0.072
50
CLF056 Cleft Lip with or Without Cleft Palate 47 0.072
51
ISL109 Isolated Cleft Lip 38 0.072
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