Search results for congenital disorder of glycosylation type 1a

174 hits were found for congenital disorder of glycosylation type 1a

# Family MCID Name MIFTS Score
1
c CNG415 Congenital Disorder of Glycosylation, Type Ia 53 4.707
2
c CNG206 Congenital Disorder of Glycosylation, Type Ie 40 4.327
3
PMM002 Pmm2-Congenital Disorder of Glycosylation 14 2.804
4
c BLD140 Blood Group, I System 37 0.543
5
P DBT009 Diabetes Mellitus 72 0.433
6
P HPT021 Hepatitis 75 0.373
7
P LKM002 Leukemia 75 0.355
8
P CNG411 Congenital Disorder of Glycosylation, Type in 55 0.346
9
AGN016 Aging 65 0.310
10
END072 Endotheliitis 46 0.306
11
P BRS047 Breast Cancer 100 0.299
12
P NRP001 Neuropathy 63 0.297
13
P MSC005 Muscular Dystrophy 66 0.295
14
NRN002 Neuronitis 43 0.295
15
P LYM118 Lymphoma 71 0.294
16
P HRT032 Heart Disease 80 0.271
17
P THY032 Thyroiditis 56 0.263
18
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.261
19
P PNC044 Pancreatitis 64 0.261
20
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.260
21
ATM095 Autoimmune Disease 66 0.254
22
PRS047 Prostatitis 59 0.253
23
P ADN016 Adenocarcinoma 71 0.246
24
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.244
25
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.244
26
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.244
27
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.244
28
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.244
29
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.244
30
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.244
31
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.244
32
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.244
33
P ANR048 Aniridia 1 68 0.242
34
P ART022 Arthritis 77 0.241
35
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.236
36
P SCH015 Schizophrenia 71 0.232
37
ANR038 Anorexia Nervosa 1 21 0.226
38
BLD137 Blood Group--Ahonen 17 0.226
39
P LNG032 Lung Cancer 99 0.224
40
RTN023 Retinitis 52 0.222
41
P MLT020 Multiple Sclerosis 85 0.220
42
P ENC018 Encephalopathy 58 0.213
43
MLN008 Melanoma 72 0.212
44
P GLY013 Glycogen Storage Disease 61 0.210
45
P PRS040 Prostate Cancer 88 0.209
46
P HYP265 Hypotonia 40 0.207
47
P LVR013 Liver Disease 76 0.205
48
P HPT023 Hepatocellular Carcinoma 94 0.205
49
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.204
50
P CRV039 Cervicitis 49 0.202
51
ALR002 Al-Raqad Syndrome 30 0.202
52
MSC165 Muscular Dystrophy, Congenital, Lmna-Related 59 0.197
53
P EPL164 Epilepsy 70 0.194
54
P MYP004 Myopathy 69 0.192
55
SQM006 Squamous Cell Carcinoma 74 0.192
56
P RHM011 Rheumatoid Arthritis 91 0.191
57
P CLR023 Colorectal Cancer 98 0.187
58
P HYP086 Hypothyroidism 62 0.186
59
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.184
60
P INF038 Influenza 77 0.184
61
P MYC007 Myocardial Infarction 81 0.180
62
c HPT001 Hepatitis C 73 0.180
63
P NRV007 Nervous System Disease 75 0.179
64
HYP056 Hypoglycemia 62 0.179
65
ISC004 Ischemia 66 0.170
66
P CTR002 Cataract 60 0.169
67
ADN018 Adenoma 63 0.168
68
P ESP024 Esophagitis 64 0.167
69
SRC014 Sarcoma 68 0.163
70
LNG099 Lung Disease 67 0.162
71
P OVR042 Ovarian Cancer 82 0.160
72
HYP266 Hypoxia 61 0.157
73
c CNT035 Central Nervous System Disease 65 0.157
74
DMN002 Dementia 68 0.156
75
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 14 0.155
76
HPT082 Hepatic Adenomas, Familial 52 0.153
77
P TCL004 T-Cell Leukemia 50 0.152
78
URN009 Urinary System Disease 58 0.151
79
P MYL006 Myeloid Leukemia 69 0.150
80
CYS001 Cystic Fibrosis 85 0.149
81
P PNM007 Pneumonia 70 0.147
82
ALP046 Alport Syndrome, X-Linked 74 0.147
83
P PNC035 Pancreatic Cancer 89 0.145
84
P THR014 Thrombocytopenia 65 0.145
85
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.143
86
P LPS004 Lupus Erythematosus 69 0.143
87
P BCL006 B-Cell Lymphomas 70 0.143
88
P NRB001 Neuroblastoma 73 0.142
89
P CRN300 Coronary Heart Disease 1 57 0.140
90
P MYC084 Mycobacterium Tuberculosis 1 69 0.139
91
P DRR001 Diarrhea 60 0.138
92
c SYS001 Systemic Lupus Erythematosus 86 0.136
93
HYP066 Hyperglycemia 64 0.136
94
P INF032 Infertility 59 0.135
95
P RNG031 Ring Chromosome Y Syndrome 29 0.133
96
EPD016 Epidermolysis Bullosa 57 0.133
97
c HPT003 Hepatitis a 63 0.130
98
P PLY019 Polyneuropathy 58 0.129
99
c HPT016 Hepatitis B 68 0.128
100
P DYS154 Dystonia 61 0.128
101
c LKM061 Leukemia, Acute Myeloid 81 0.127
102
OST012 Osteoarthritis 88 0.122
103
c BRN108 Branchiootic Syndrome 1 47 0.119
104
MLR004 Malaria 86 0.118
105
CLT003 Colitis 63 0.117
106
P LYM026 Lymphoblastic Leukemia 66 0.117
107
P GLM007 Glomerulonephritis 61 0.114
108
MYL069 Myeloma, Multiple 86 0.114
109
c ACT075 Acute Myocardial Infarction 64 0.112
110
DFF005 Diffuse Large B-Cell Lymphoma 64 0.111
111
P BLD051 Blood Coagulation Disease 38 0.110
112
P BLD134 Bladder Cancer 78 0.109
113
RCK004 Rickets 63 0.109
114
P DLT002 Dilated Cardiomyopathy 76 0.109
115
RTN018 Retinal Disease 56 0.108
116
P ICH004 Ichthyosis 54 0.108
117
P MYS005 Myositis 63 0.107
118
P LMB006 Limb-Girdle Muscular Dystrophy 55 0.104
119
LVR012 Liver Cirrhosis 73 0.102
120
P MCR010 Microcephaly 57 0.102
121
P HYP061 Hypertrophic Cardiomyopathy 65 0.101
122
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.100
123
LRY026 Laryngeal Cleft 25 0.100
124
ALB002 Albinism 45 0.100
125
MCS002 Mucositis 61 0.098
126
DWR001 Dwarfism 48 0.096
127
P RSP003 Respiratory Failure 71 0.096
128
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.095
129
IMM158 Immune Suppression 57 0.094
130
c BLM008 Bulimia Nervosa 2 53 0.094
131
PLC008 Placenta Disease 48 0.093
132
P MYS003 Myasthenia Gravis 73 0.092
133
ACR006 Aceruloplasminemia 65 0.091
134
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.090
135
DBT010 Diabetic Neuropathy 60 0.089
136
MTC069 Mitochondrial Disorders 49 0.089
137
P CNG001 Congenital Myasthenic Syndrome 55 0.087
138
P PMP001 Pemphigus 55 0.087
139
CRB045 Cerebellar Hypoplasia 48 0.086
140
ORL011 Oral Cancer 60 0.085
141
WST005 West Nile Virus 58 0.084
142
SPN041 Spinal Cord Disease 54 0.084
143
P CRN037 Craniosynostosis 68 0.084
144
HMG005 Hemoglobinopathy 53 0.084
145
PHR003 Pharyngitis 59 0.083
146
P EPD003 Epidermolysis Bullosa Simplex 53 0.083
147
P RTT002 Rett Syndrome 82 0.083
148
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.082
149
P INT143 Interstitial Cystitis 63 0.082
150
P CYS018 Cystitis 57 0.081
151
INS001 Insulinoma 66 0.080
152
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 57 0.080
153
GST040 Gastric Adenocarcinoma 60 0.079
154
BLD163 Blood Group, Dombrock System 23 0.079
155
HMS001 Hemosiderosis 50 0.078
156
ICH002 Ichthyosis Bullosa of Siemens 48 0.076
157
P AGM001 Agammaglobulinemia 70 0.075
158
c MYS011 Myasthenia Gravis Congenital 28 0.074
159
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 53 0.073
160
CHL109 Childhood Apraxia of Speech 31 0.071
161
P EPL140 Epilepsy, Idiopathic Generalized 58 0.069
162
SCH014 Schistosomiasis 62 0.069
163
c SVR001 Severe Acute Respiratory Syndrome 58 0.068
164
IGR001 Ige Responsiveness, Atopic 56 0.067
165
c MSC035 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 52 0.067
166
WLK001 Walker-Warburg Syndrome 59 0.066
167
P HYP035 Hypophosphatasia 58 0.063
168
c MSC042 Muscular Dystrophy-Dystroglycanopathy , Type B, 6 49 0.063
169
c SPN393 Spinal Muscular Atrophy, Type I 50 0.062
170
ANT009 Antithrombin Iii Deficiency 58 0.062
171
HYP017 Hypophosphatemia 45 0.060
172
MSC077 Muscle Eye Brain Disease 51 0.057
173
c MSC036 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 57 0.053
174
CHN016 Cohen Syndrome 48 0.045
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