Search results for ITM2B

21 hits were found for ITM2B

# Family MCID Name MIFTS Score
2
RTN170 Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Abnormalities 19 6.389
4
P DMN002 Dementia 66 4.923
5
P ALZ034 Alzheimer Disease 88 4.418
7
P AMY004 Amyloidosis 70 3.756
9
c CNG021 Congenital Toxoplasmosis 54 2.168
10
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 49 2.168
11
P GRN048 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative 48 2.168
12
SCK001 Sick Building Syndrome 34 2.168
13
TNF001 Tinea Favosa 33 2.168
14
VRL002 Variola Minor 25 2.168
15
FND002 Fundus Dystrophy 55 0.128
16
c INH030 Inherited Retinal Disorder 51 0.128
17
P LYM118 Lymphoma 68 0.090
18
GT001 Gout 64 0.090
19
P BCL017 B-Cell Lymphoma 58 0.090
20
P RTN018 Retinal Disease 53 0.090
21
HYP014 Hyperuricemia 52 0.090
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