Search results for mitochondrial neurogastrointestinal encephalomyopathy syndrome

46 hits were found for mitochondrial neurogastrointestinal encephalomyopathy syndrome

# Family MCID Name MIFTS Score
1
MTC061 Mitochondrial Dna Depletion Syndrome 1 36 5.427
2
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 30 4.603
3
P ENC011 Encephalomyopathy 37 0.900
4
P MTC004 Mitochondrial Encephalomyopathy 43 0.526
5
P LCT001 Lactic Acidosis 50 0.348
6
P MTC069 Mitochondrial Disorders 55 0.329
7
P MYP004 Myopathy 68 0.283
8
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 27 0.281
9
P NRP001 Neuropathy 57 0.246
10
CRB009 Cerebritis 39 0.244
11
P ENC018 Encephalopathy 52 0.238
12
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 0.204
13
KRN002 Kearns-Sayre Syndrome 57 0.197
14
AND005 Androgen Insensitivity Syndrome, Mild 16 0.157
15
HYP080 Hypogonadism 52 0.154
16
MTC028 Mitochondrial Cardiomyopathy 32 0.153
17
P NRV007 Nervous System Disease 70 0.142
18
MTC005 Mitochondrial Metabolism Disease 38 0.140
19
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 28 0.138
20
P MSC005 Muscular Dystrophy 65 0.137
21
PRT036 Peritonitis 60 0.136
22
c INT072 Intestinal Pseudo-Obstruction 41 0.134
23
P ESP024 Esophagitis 59 0.134
24
CMB019 Combined Oxidative Phosphorylation Deficiency 8 32 0.132
25
P ANR007 Anorexia Nervosa 60 0.122
26
HPT074 Hepatic Adenoma, Somatic 44 0.121
27
MTC097 Mitochondrial Complex Iv Deficiency 51 0.111
28
P END033 Endocarditis 53 0.108
29
ETN001 Eating Disorder 56 0.107
30
P CLC005 Celiac Disease 69 0.107
31
PLY020 Polyradiculoneuropathy 45 0.103
32
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 42 0.102
33
TRG002 Trigeminal Neuralgia 56 0.099
34
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 43 0.099
35
DVR002 Diverticulitis 42 0.098
36
BRN097 Brainstem Auditory Evoked Responses 22 0.095
37
RFR013 Refractory Celiac Disease 33 0.093
38
SPN060 Spondylocarpotarsal Synostosis Syndrome 40 0.079
39
P EPS003 Episodic Ataxia 54 0.073
40
P INF016 Infantile Epileptic Encephalopathy 44 0.073
41
c ANR038 Anorexia Nervosa 1 27 0.072
42
HYP264 Hypertonia 35 0.071
43
c SPN293 Spinocerebellar Ataxia 12 52 0.066
44
ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 23 0.064
45
EPS004 Episodic Ataxia/myokymia Syndrome 45 0.063
46
UND011 Undetermined Early-Onset Epileptic Encephalopathy 19 0.060
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