Search results for "congenital disorder of glycosylation type 1a"

The MalaCard for "congenital disorder of glycosylation type 1a" has been retired.
Searching MalaCards for entries containing "congenital disorder of glycosylation type 1a"

150 hits were found for 'congenital disorder of glycosylation type 1a'

# Family MCID Name MIFTS Score
1
c CNG415 Congenital Disorder of Glycosylation, Type Ia 45 4.520
2
PMM002 Pmm2-Congenital Disorder of Glycosylation 9 2.748
3
P HPT021 Hepatitis 69 0.354
4
P LKM002 Leukemia 71 0.342
5
END072 Endotheliitis 42 0.299
6
NRN002 Neuronitis 41 0.288
7
P BRS047 Breast Cancer 100 0.283
8
P MSC005 Muscular Dystrophy 65 0.283
9
P LYM118 Lymphoma 69 0.282
10
P NRP001 Neuropathy 59 0.277
11
P OBS005 Obesity 92 0.262
12
P HRT032 Heart Disease 75 0.258
13
P THY032 Thyroiditis 54 0.256
14
PRS047 Prostatitis 56 0.250
15
P PNC044 Pancreatitis 61 0.248
16
P ADN016 Adenocarcinoma 69 0.232
17
P ART022 Arthritis 75 0.229
18
ALR002 Al-Raqad Syndrome 36 0.227
19
P SCH015 Schizophrenia 77 0.223
20
P LNG032 Lung Cancer 95 0.215
21
P HPT023 Hepatocellular Carcinoma 92 0.212
22
RTN023 Retinitis 50 0.211
23
MLN008 Melanoma 62 0.210
24
P MYP004 Myopathy 67 0.208
25
P PRS040 Prostate Cancer 90 0.205
26
P ENC018 Encephalopathy 59 0.200
27
P ATX004 Ataxia 53 0.198
28
HV1006 Hiv-1 80 0.195
29
P GLY013 Glycogen Storage Disease 60 0.193
30
P EPL164 Epilepsy 66 0.193
31
SQM006 Squamous Cell Carcinoma 70 0.192
32
P RHM011 Rheumatoid Arthritis 89 0.190
33
P LVR013 Liver Disease 75 0.188
34
P CLR023 Colorectal Cancer 97 0.185
35
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.185
36
P CRV039 Cervicitis 45 0.183
37
P HYP265 Hypotonia 38 0.181
38
c HPT001 Hepatitis C 68 0.178
39
P CRD011 Cardiomyopathy 68 0.177
40
P MYC007 Myocardial Infarction 79 0.177
41
ATM052 Autoimmune Disease 1 25 0.177
42
P INF038 Influenza 72 0.176
43
HYP056 Hypoglycemia 61 0.169
44
P OVR042 Ovarian Cancer 76 0.165
45
P ESP024 Esophagitis 61 0.165
46
ADN018 Adenoma 58 0.164
47
MTH009 Mouth Disease 61 0.163
48
PHY002 Physical Disorder 43 0.163
49
ACR041 Acromelic Frontonasal Dysostosis 45 0.161
50
BRT030 Birth Defects 43 0.160
51
SRC014 Sarcoma 66 0.158
52
ISC004 Ischemia 61 0.157
53
P CTR002 Cataract 58 0.157
54
DMN002 Dementia 65 0.156
55
HYP266 Hypoxia 56 0.154
56
ATH003 Atherosclerosis 65 0.151
57
ATM053 Autoimmune Disease 2 16 0.151
58
P NRV007 Nervous System Disease 71 0.149
59
P MSC033 Muscle Disorders 52 0.147
60
CYS001 Cystic Fibrosis 83 0.147
61
c HMG001 Hemoglobin C Disease 47 0.146
62
P MYL006 Myeloid Leukemia 66 0.144
63
SKN016 Skin Disease 66 0.144
64
MSC004 Muscle Tissue Disease 34 0.143
65
c HPT016 Hepatitis B 65 0.141
66
P LPS004 Lupus Erythematosus 64 0.140
67
P PNC035 Pancreatic Cancer 87 0.140
68
P NRB001 Neuroblastoma 70 0.138
69
P THR014 Thrombocytopenia 64 0.137
70
c SYS001 Systemic Lupus Erythematosus 86 0.135
71
ATM054 Autoimmune Disease 3 15 0.133
72
HPT074 Hepatic Adenoma, Somatic 50 0.133
73
c INH020 Inherited Metabolic Disorder 49 0.133
74
P DRR001 Diarrhea 60 0.132
75
HYP066 Hyperglycemia 61 0.131
76
HNM002 Hinman Syndrome 25 0.131
77
CSY001 C Syndrome 50 0.130
78
EPD016 Epidermolysis Bullosa 57 0.129
79
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.129
80
P PLY019 Polyneuropathy 56 0.125
81
P INF032 Infertility 59 0.125
82
ATM055 Autoimmune Disease 4 15 0.120
83
AND005 Androgen Insensitivity Syndrome, Mild 16 0.119
84
P OST012 Osteoarthritis 83 0.118
85
PRD011 Proud Syndrome 42 0.117
86
CLT003 Colitis 60 0.117
87
ORL011 Oral Cancer 56 0.117
88
c ACT075 Acute Myocardial Infarction 60 0.115
89
ATP002 Atopy 66 0.115
90
VND001 Vein Disease 47 0.114
91
MLR004 Malaria 83 0.114
92
P DYS154 Dystonia 65 0.113
93
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.113
94
P GLM007 Glomerulonephritis 59 0.113
95
P LYM026 Lymphoblastic Leukemia 62 0.112
96
RTN018 Retinal Disease 53 0.111
97
P RSP003 Respiratory Failure 71 0.111
98
P RCK004 Rickets 61 0.108
99
ALC007 Alcohol Dependence 63 0.105
100
P ICH004 Ichthyosis 52 0.103
101
LYM019 Lymphosarcoma 53 0.101
102
ATR060 Atrial Standstill, Digenic 51 0.099
103
PLC008 Placenta Disease 33 0.099
104
LVR012 Liver Cirrhosis 67 0.099
105
P MYS005 Myositis 57 0.098
106
P ANR007 Anorexia Nervosa 61 0.098
107
P LMB006 Limb-Girdle Muscular Dystrophy 51 0.097
108
ALB002 Albinism 46 0.097
109
DWR001 Dwarfism 47 0.095
110
c DLT002 Dilated Cardiomyopathy 76 0.095
111
P MCR010 Microcephaly 58 0.094
112
MCS002 Mucositis 55 0.094
113
P CRB042 Cerebellar Ataxia 63 0.092
114
ADP007 Adie Pupil 34 0.092
115
P MYS003 Myasthenia Gravis 67 0.091
116
P INT143 Interstitial Cystitis 57 0.089
117
PHR003 Pharyngitis 56 0.089
118
P PLM036 Pulmonary Fibrosis 71 0.088
119
DBT010 Diabetic Neuropathy 55 0.085
120
PMP001 Pemphigus 50 0.084
121
P CNG001 Congenital Myasthenic Syndrome 55 0.083
122
P CRN037 Craniosynostosis 66 0.082
123
P EPD003 Epidermolysis Bullosa Simplex 53 0.082
124
P CYS018 Cystitis 52 0.081
125
P RTT002 Rett Syndrome 77 0.080
126
INS001 Insulinoma 61 0.079
127
LRY026 Laryngeal Cleft 27 0.077
128
CRB045 Cerebellar Hypoplasia 48 0.077
129
CNG008 Congenital Ichthyosiform Erythroderma 56 0.076
130
MYC033 Myoclonus 42 0.076
131
P NSP012 Nasopharyngeal Carcinoma 66 0.074
132
ICH002 Ichthyosis Bullosa of Siemens 45 0.073
133
P CNG046 Congenital Fiber-Type Disproportion 50 0.073
134
P AGM001 Agammaglobulinemia 64 0.073
135
CNG065 Congenital Contractures 29 0.071
136
CRV038 Cervical Squamous Cell Carcinoma 60 0.071
137
CHN016 Cohen Syndrome 54 0.066
138
DBT008 Diabetic Angiopathy 44 0.066
139
HYP020 Hyperprolactinemia 60 0.066
140
PRX034 Peroxisome Disorders 39 0.061
141
P HYP035 Hypophosphatasia 57 0.060
142
P LNG064 Lung Cancer Susceptibility 3 62 0.060
143
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.056
144
P ART121 Arthrogryposis Multiplex Congenita, Distal, Type 1 42 0.056
145
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 40 0.056
146
MTL002 Metal Metabolism Disorder 35 0.056
147
PBL001 Piebaldism 57 0.052
148
P CHN044 Chondrodysplasia Punctata Syndrome 36 0.047
149
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 48 0.044
150
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 52 0.038