Search results for rab7b

51 hits were found for rab7b

# Family MCID Name MIFTS Score
1
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 58 12.220
2
P PRK057 Parkinson Disease, Late-Onset 80 10.753
3
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 67 9.978
4
c AMY091 Amyotrophic Lateral Sclerosis 1 88 9.978
5
CHR629 Charcot-Marie-Tooth Disease and Deafness 50 9.978
6
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 58 9.978
7
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 50 7.055
8
P RTN008 Retinitis Pigmentosa 80 7.055
9
c FRN059 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7 47 7.055
10
NRP049 Neuropathy, Hereditary Sensory and Autonomic, Type I, with Cough and Gastroesophageal Reflux 32 7.055
11
VCS001 Vici Syndrome 57 7.055
12
c CHR353 Charcot-Marie-Tooth Disease, Axonal, Type 2l 41 7.055
13
c NRP039 Neuropathy, Hereditary Sensory, Type Id 39 7.055
14
P WRB001 Warburg Micro Syndrome 41 7.055
15
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 7.055
16
c CTR095 Cataract 8, Multiple Types 35 7.055
17
P HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 48 7.055
18
c CHR519 Charcot-Marie-Tooth Disease, Type 4b2 48 7.055
19
c CHR420 Charcot-Marie-Tooth Disease, Type 4j 48 7.055
20
LGN006 Legionnaire Disease 52 7.055
21
CSY001 C Syndrome 61 7.055
22
c NMN015 Niemann-Pick Disease, Type C1 68 7.055
23
c LKD023 Leukodystrophy, Hypomyelinating, 12 38 7.055
24
c CHR422 Charcot-Marie-Tooth Disease, Dominant Intermediate B 46 7.055
25
P GRS003 Griscelli Syndrome 53 7.055
26
DSS008 Disease of Mental Health 74 7.055
27
P HRM001 Hermansky-Pudlak Syndrome 65 7.055
28
NRM005 Neuromuscular Disease 63 7.055
29
P CHR071 Charcot-Marie-Tooth Disease 64 7.055
30
P NMN002 Niemann-Pick Disease 60 7.055
31
P PRP019 Peripheral Nervous System Disease 58 7.055
32
CHL014 Cholera 62 3.741
33
STM007 Stomatitis 54 3.741
34
ACT119 Acute Promyelocytic Leukemia 62 3.292
35
P MNC007 Monocytic Leukemia 47 3.292
36
CRB004 Cerebral Artery Occlusion 45 3.033
37
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 2.892
38
P HML001 Hemolytic-Uremic Syndrome 52 2.740
39
c SYS001 Systemic Lupus Erythematosus 87 2.574
40
CYT002 Cytokine Deficiency 43 2.574
41
P DMN002 Dementia 66 1.732
42
P INF037 Inflammatory Bowel Disease 53 1.617
43
P ALZ034 Alzheimer Disease 87 1.549
44
DYS015 Dysentery 50 1.342
45
CYS001 Cystic Fibrosis 78 1.096
46
CLT003 Colitis 63 1.096
47
DMN031 Dementia, Lewy Body 65 0.775
48
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.775
49
APP009 Appendix Adenocarcinoma 45 0.775
50
MCN001 Mucinous Adenocarcinoma 49 0.775
51
P BRS047 Breast Cancer 98 0.642
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