Search results for mitochondrial neurogastrointestinal encephalomyopathy syndrome

45 hits were found for mitochondrial neurogastrointestinal encephalomyopathy syndrome

# Family MCID Name MIFTS Score
1
MTC061 Mitochondrial Dna Depletion Syndrome 1 35 6.028
2
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 39 5.797
3
P ENC011 Encephalomyopathy 40 1.053
4
MTC069 Mitochondrial Disorders 49 0.331
5
P MYP004 Myopathy 69 0.321
6
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 28 0.298
7
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.294
8
P ENC018 Encephalopathy 58 0.288
9
P MTC133 Mitochondrial Myopathy 53 0.281
10
CRB009 Cerebritis 41 0.279
11
P NRP001 Neuropathy 63 0.277
12
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.265
13
AGN016 Aging 65 0.256
14
KRN002 Kearns-Sayre Syndrome 59 0.245
15
MTC005 Mitochondrial Metabolism Disease 33 0.221
16
P ANR048 Aniridia 1 68 0.221
17
ANR038 Anorexia Nervosa 1 21 0.219
18
BLD137 Blood Group--Ahonen 17 0.219
19
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.207
20
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.199
21
HYP080 Hypogonadism 54 0.177
22
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.174
23
P ESP024 Esophagitis 64 0.159
24
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 0.159
25
PRT036 Peritonitis 67 0.157
26
P MSC005 Muscular Dystrophy 66 0.157
27
c INT072 Intestinal Pseudo-Obstruction 57 0.156
28
P NRV007 Nervous System Disease 75 0.152
29
P END033 Endocarditis 58 0.124
30
c 3MT014 3-Methylglutaconic Aciduria, Type V 40 0.119
31
PLY020 Polyradiculoneuropathy 48 0.118
32
TRG002 Trigeminal Neuralgia 60 0.117
33
ETN001 Eating Disorder 61 0.115
34
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 46 0.113
35
c BLM008 Bulimia Nervosa 2 53 0.112
36
DVR002 Diverticulitis 44 0.111
37
OCL011 Ocular Motility Disease 31 0.111
38
BRN097 Brainstem Auditory Evoked Responses 24 0.109
39
c PRM196 Premature Ovarian Failure 1 68 0.108
40
RFR013 Refractory Celiac Disease 34 0.106
41
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 30 0.098
42
SPN060 Spondylocarpotarsal Synostosis Syndrome 41 0.091
43
P CLC063 Celiac Disease 1 65 0.090
44
PRL008 Paralytic Ileus 38 0.078
45
NNT041 Neonatal Period Electroclinical Syndrome 21 0.078
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