Search results for GALNS

178 hits were found for GALNS

# Family MCID Name MIFTS Score
1
c MCP047 Mucopolysaccharidosis, Type Iva 62 102.588
2
c MCP004 Mucopolysaccharidosis Iv 61 63.382
3
P MRQ003 Morquio Syndrome 35 41.844
4
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 25.872
5
c ACT134 Acute Liver Failure 59 23.041
6
LYS002 Lysosomal Storage Disease 51 19.293
7
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 16.760
8
ODN023 Odontochondrodysplasia 67 11.479
9
P ZLL001 Zellweger Syndrome 65 10.665
10
c GM1007 Gm1 Gangliosidosis 65 10.665
11
SCH036 Scheie Syndrome 73 9.851
12
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 9.652
13
ATS010 Autosomal Recessive Disease 42 9.314
14
GLC012 Galactosialidosis 56 8.692
15
c MCP048 Mucopolysaccharidosis, Type Ivb 52 8.668
16
LGG001 Legg-Calve-Perthes Disease 60 7.963
17
P GNG009 Gangliosidosis 44 7.963
18
MLT135 Multiple Sulfatase Deficiency 53 7.780
19
P MCL001 Mucolipidosis 49 7.780
20
c MCP052 Mucopolysaccharidosis, Type Vi 67 7.541
21
FCS002 Fucosidosis 62 6.966
22
HRL003 Hurler Syndrome 66 6.966
23
c MCP050 Mucopolysaccharidosis, Type Ii 74 6.966
24
c MCP044 Mucopolysaccharidosis, Type Iiib 59 6.966
25
c MCP045 Mucopolysaccharidosis, Type Iiic 59 6.966
26
c MCP046 Mucopolysaccharidosis, Type Iiid 50 6.966
27
c MCP049 Mucopolysaccharidosis, Type Vii 63 6.966
28
c MCL062 Mucolipidosis Ii Alpha/beta 68 6.966
29
c MCP043 Mucopolysaccharidosis, Type Iiia 61 6.966
30
ISL114 Isolated Growth Hormone Deficiency, Type Ii 39 6.966
31
TRC097 Tracheomalacia 43 6.966
32
TRC026 Tracheal Disease 43 6.966
33
P BND014 Bone Development Disease 33 6.966
34
OST016 Osteochondrosis 52 6.966
35
GLY031 Glycoproteinosis 49 6.966
36
c MCP001 Mucopolysaccharidosis Iii 69 6.966
37
DHY008 Dihydroxyadeninuria 24 6.334
38
TXC005 Toxic Shock Syndrome 62 4.984
39
48X005 48,xyyy 39 4.764
40
MCP033 Mucopolysaccharidoses 44 4.325
41
HPT004 Hepatic Coma 43 4.278
42
HPT019 Hepatic Encephalopathy 59 4.182
43
P LVR013 Liver Disease 69 4.150
44
FTT001 Fatty Liver Disease 62 4.033
45
CYT002 Cytokine Deficiency 43 3.987
46
c VRL010 Viral Hepatitis 53 3.860
47
P HPT021 Hepatitis 69 3.817
48
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.767
49
PRT036 Peritonitis 65 3.152
50
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 2.930
51
P ENC018 Encephalopathy 62 2.819
52
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.405
53
DSS009 Disseminated Intravascular Coagulation 57 2.302
54
DWR001 Dwarfism 44 2.300
55
P BCL017 B-Cell Lymphoma 59 2.187
56
c HPT001 Hepatitis C 62 2.153
57
PCT001 Pectus Carinatum 33 2.153
58
BCT022 Bacterial Infectious Disease 56 2.075
59
c HPT003 Hepatitis a 63 2.075
60
ODN022 Odontoid Hypoplasia 17 1.993
61
P GST044 Gastritis 55 1.993
62
LVR012 Liver Cirrhosis 63 1.993
63
LYS030 Lysosomal Storage Disease with Skeletal Involvement 15 1.909
64
DYS018 Dysostosis 44 1.909
65
c HPT016 Hepatitis B 62 1.909
66
P MYC084 Mycobacterium Tuberculosis 1 68 1.820
67
CHD004 Chudley-Mccullough Syndrome 48 1.820
68
PST092 Posttransplant Acute Limbic Encephalitis 28 1.820
69
TLR001 Tularemia 56 1.820
70
URL001 Urolithiasis 46 1.726
71
c HNT010 Huntington Disease-Like 1 55 1.726
72
c HNT011 Huntington Disease-Like 3 34 1.726
73
c HPT073 Hepatitis C Virus 71 1.726
74
c HNT004 Huntington Disease-Like 2 52 1.726
75
P HYP098 Hypereosinophilic Syndrome 66 1.726
76
P CHR012 Chronic Granulomatous Disease 69 1.726
77
PTT037 Pituitary Tumors 44 1.726
78
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.628
79
HPT014 Hepatorenal Syndrome 49 1.628
80
HYP056 Hypoglycemia 65 1.628
81
c TYP008 Type 1 Diabetes Mellitus 70 1.591
82
c TYP030 Type 1 Diabetes Mellitus 4 21 1.591
83
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.523
84
P FBR017 Fibrosarcoma 56 1.523
85
c ACT071 Acute Kidney Failure 60 1.523
86
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.410
87
ALL029 Allergic Disease 59 1.410
88
CHL068 Cholestasis 61 1.410
89
MTR087 Maternal Uniparental Disomy 28 1.287
90
P GLL020 Gallbladder Disease 56 1.287
91
PRT037 Pertussis 65 1.287
92
ANX004 Anoxia 40 1.151
93
c GLY008 Glycogen Storage Disease Ii 72 1.151
94
HRT012 Heart Valve Disease 53 1.151
95
ALC006 Alcoholic Hepatitis 61 1.151
96
P GCH001 Gaucher's Disease 70 1.151
97
SVR004 Severe Combined Immunodeficiency 72 1.151
98
P ADL010 Adult Respiratory Distress Syndrome 71 1.151
99
PLM010 Pulmonary Edema 55 1.151
101
CLN015 Colon Adenocarcinoma 65 1.080
102
QLT002 Qualitative or Quantitative Defects of Dystrophin 19 0.997
103
SPN186 Spinal Cord Injury 61 0.997
104
INS024 Insulin-Like Growth Factor I 78 0.997
105
ANX010 Anxiety 70 0.997
106
KWS002 Kawasaki Disease 65 0.997
107
VRC005 Varicose Veins 60 0.997
108
HPT067 Hepatocellular Adenoma 43 0.997
109
P HMR005 Hemorrhoid 49 0.997
110
SHW001 Shwartzman Phenomenon 36 0.997
111
HYP066 Hyperglycemia 61 0.997
112
c HPT015 Hepatitis D 49 0.997
113
P CRD119 Cardiac Arrest 67 0.997
114
DYS032 Dystrophinopathies 47 0.997
115
DPR016 Depression 65 0.997
116
MRQ002 Morquio Syndrome C 13 0.889
117
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 0.814
118
ALP077 Alpha-Methylacetoacetic Aciduria 52 0.814
119
FBR012 Fabry Disease 70 0.814
120
OTT002 Otitis Media 71 0.814
121
P SLP006 Sleep Apnea 69 0.814
122
KSH004 Kashin-Beck Disease 38 0.814
123
INF034 Infective Endocarditis 54 0.814
124
NNL006 Non-Alcoholic Steatohepatitis 54 0.814
125
P ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 27 0.814
126
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.814
127
P SCL018 Scoliosis 57 0.814
128
ARG004 Argyria 26 0.814
129
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.814
130
P KDN018 Kidney Disease 72 0.814
131
P DYS154 Dystonia 64 0.814
132
LYM027 Lymphopenia 56 0.814
133
P ART022 Arthritis 71 0.814
134
P MNC007 Monocytic Leukemia 47 0.814
135
NRG002 Neurogenic Bladder 55 0.814
136
MTR002 Mitral Valve Insufficiency 52 0.814
137
P END033 Endocarditis 58 0.814
138
BRN024 Bronchitis 67 0.814
139
P RHN004 Rhinitis 57 0.814
140
P CHR345 Chronic Pain 50 0.814
141
BRN071 Brain Injury 50 0.814
142
MCL022 Mucolipidoses 33 0.814
143
HPS001 Hip Subluxation 16 0.814
144
P BRS047 Breast Cancer 98 0.811
145
P AVS003 Avascular Necrosis 41 0.575
146
SPS057 Spasticity 42 0.575
147
MND023 Mend Syndrome 49 0.575
148
P LPR021 Leprosy 3 71 0.575
149
c BLD146 Blood Group, P1pk System 28 0.575
150
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.575
151
CYS001 Cystic Fibrosis 78 0.575
152
P INF037 Inflammatory Bowel Disease 53 0.575
153
P ASP006 Aspergillosis 72 0.575
154
c EXS019 Exostoses, Multiple, Type I 54 0.575
155
EXT007 Extracutaneous Mastocytoma 38 0.575
156
MST004 Mast Cell Neoplasm 42 0.575
157
TRC003 Trichomoniasis 53 0.575
158
VCC001 Vaccinia 47 0.575
159
c VRL007 Viral Encephalitis 50 0.575
160
CNN005 Connective Tissue Disease 67 0.575
161
P CTR002 Cataract 60 0.575
162
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.575
163
P GRF003 Graft-Versus-Host Disease 71 0.575
164
OST003 Osteonecrosis 61 0.575
165
P NRN021 Neuronal Ceroid Lipofuscinosis 65 0.575
166
MST005 Mastitis 53 0.575
167
P SLP005 Sleep Disorder 61 0.575
168
PLG002 Plague 58 0.575
169
SQM006 Squamous Cell Carcinoma 60 0.575
170
STM007 Stomatitis 54 0.575
171
HNS001 Hansen's Disease 32 0.575
172
c CHR417 Chronic Graft Versus Host Disease 55 0.575
173
P PNC035 Pancreatic Cancer 86 0.573
174
CLL010 Cellular Ependymoma 57 0.573
175
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.504
176
c CLR087 Colorectal Cancer 12 34 0.504
177
GST103 Gastric Cancer, Hereditary Diffuse 68 0.504
178
SML009 Small Intestine Adenocarcinoma 57 0.504
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