Search results for lmnb2

29 hits were found for lmnb2

# Family MCID Name MIFTS Score
1
c EPL154 Epilepsy, Progressive Myoclonic, 9 25 15.370
2
c LPD019 Lipodystrophy, Partial, Acquired 43 7.000
3
P GST053 Gastric Cancer 83 3.998
4
P EPL164 Epilepsy 71 3.998
5
c PRG146 Progressive Myoclonus Epilepsy 9 9 3.170
6
c PRG011 Progressive Myoclonus Epilepsy 42 2.882
7
P MSC005 Muscular Dystrophy 66 2.827
9
P EMR001 Emery-Dreifuss Muscular Dystrophy 61 2.827
10
c ACQ043 Acquired Lipodystrophy 27 2.827
11
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.999
12
P CHR071 Charcot-Marie-Tooth Disease 64 1.999
13
c EMR018 Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant 54 1.999
14
c CRD093 Cardiomyopathy, Dilated, 1a 52 1.999
15
MSC190 Muscular Disease 51 1.999
16
P PLG001 Pelger-Huet Anomaly 50 1.999
17
RYN003 Reynolds Syndrome 47 1.999
18
c EMR020 Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive 46 1.999
19
LKD025 Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 44 1.999
20
c CHR650 Charcot-Marie-Tooth Disease, Axonal, Type 2b1 44 1.999
21
c LPD030 Lipodystrophy, Familial Partial, Type 5 43 1.999
22
c CRD069 Cardiomyopathy, Dilated, 1h 29 1.999
23
NNN001 Nonencapsulated Sclerosing Carcinoma 26 1.999
24
MSC004 Muscle Tissue Disease 25 1.999
25
FTT001 Fatty Liver Disease 61 0.086
26
P MYC033 Myoclonus 46 0.086
27
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.086
28
P MYC026 Myoclonus Epilepsy 35 0.086
29
LPD043 Lipodystrophy, Partial, Acquired, with Low Complement Component C3, with or Without Glomerulonephritis 14 0.086
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