Search results for ATP1A1

169 hits were found for ATP1A1

# Family MCID Name MIFTS Score
1
c CHR678 Charcot-Marie-Tooth Disease, Axonal, Type 2dd 34 61.137
2
P HYP834 Hypomagnesemia, Seizures, and Mental Retardation 2 22 35.111
3
P CHR071 Charcot-Marie-Tooth Disease 64 17.085
4
TTH006 Tooth Disease 51 14.990
5
ADN018 Adenoma 58 14.925
6
CNN003 Conn's Syndrome 77 13.278
7
c HYP595 Hypertension, Essential 84 13.067
8
c HRD010 Hereditary Spastic Paraplegia 65 12.042
9
P ALT001 Alternating Hemiplegia of Childhood 56 8.025
10
P THY054 Thyrotoxic Periodic Paralysis 51 8.025
11
c HYP731 Hyperaldosteronism, Familial, Type I 58 7.964
12
PRS051 Parastremmatic Dwarfism 40 7.819
13
c RTN134 Retinitis Pigmentosa 40 33 7.819
14
ADR012 Adrenal Gland Disease 44 7.819
15
ADR008 Adrenal Adenoma 55 1.939
16
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.761
17
P PRS040 Prostate Cancer 95 1.715
18
ALD013 Aldosterone-Producing Adenoma 36 1.684
19
STM007 Stomatitis 52 1.579
20
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.391
21
GLM045 Glioma 62 1.294
22
GLL048 Glial Tumor 52 1.294
23
P HPT023 Hepatocellular Carcinoma 95 1.237
24
P KDN017 Kidney Cancer 60 1.235
25
DBT010 Diabetic Neuropathy 54 1.191
26
MDD018 Middle East Respiratory Syndrome 44 1.143
27
PRT036 Peritonitis 65 1.143
28
ANX010 Anxiety 70 1.116
29
P MJR001 Major Depressive Disorder 68 1.116
30
MNT002 Mental Depression 56 1.116
31
SQM006 Squamous Cell Carcinoma 59 1.116
32
DPR016 Depression 65 1.116
33
MST005 Mastitis 52 1.057
34
c TYP009 Type 2 Diabetes Mellitus 92 1.023
35
P DBT009 Diabetes Mellitus 67 1.023
36
P NRP001 Neuropathy 59 1.023
37
c FNC027 Fanconi Anemia, Complementation Group a 81 0.984
38
PRP016 Paraplegia 52 0.984
39
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 39 0.984
40
OBN001 Ouabain Resistance 15 0.938
41
P SZR006 Seizure Disorder 69 0.877
42
P BRS047 Breast Cancer 97 0.678
43
IRN008 Iron Overload in Africa 51 0.675
44
RJS001 Ruijs-Aalfs Syndrome 47 0.675
45
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.675
46
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.675
47
HPT079 Hepatoid Adenocarcinoma 39 0.675
48
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.675
49
c HPT073 Hepatitis C Virus 71 0.675
50
ADL096 Adult Hepatocellular Carcinoma 60 0.675
51
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.675
52
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.675
53
PDT042 Pediatric Hepatocellular Carcinoma 50 0.675
54
PTY007 Pityriasis Rotunda 26 0.675
55
P LNG021 Lung Occult Small Cell Carcinoma 20 0.675
56
FBR086 Fibrolamellar Carcinoma 59 0.675
57
HPT011 Hepatocellular Clear Cell Carcinoma 45 0.675
58
MYL005 Myelofibrosis 70 0.533
59
P LKM062 Leukemia, Acute Lymphoblastic 69 0.533
60
P OVR042 Ovarian Cancer 88 0.533
61
P PNC035 Pancreatic Cancer 86 0.533
62
GLB002 Glioblastoma 67 0.481
63
P FML156 Familial Hyperaldosteronism 38 0.481
64
LYM009 Lymphocytic Choriomeningitis 46 0.355
65
c ATR087 Atrial Standstill 1 74 0.290
66
ADR041 Adrenal Cortical Adenoma 48 0.290
67
SVR001 Severe Acute Respiratory Syndrome 68 0.290
68
c HYP708 Hyperaldosteronism, Familial, Type Iv 30 0.251
69
PRT251 Proteinuria, Chronic Benign 58 0.251
70
c DLT002 Dilated Cardiomyopathy 79 0.251
71
HGH043 High Grade Glioma 46 0.251
72
P OVR082 Overgrowth Syndrome 42 0.251
73
P ALZ034 Alzheimer Disease 87 0.205
74
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.205
75
c BRN108 Branchiootic Syndrome 1 63 0.205
76
ONC007 Oncocytoma 49 0.205
77
ADR016 Adrenal Cortical Carcinoma 61 0.205
78
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.205
79
P PRK039 Parkinsonism 55 0.205
80
c MGR028 Migraine with or Without Aura 1 64 0.205
81
OTT002 Otitis Media 71 0.205
82
FRY002 Fryns Syndrome 39 0.205
83
P ANP001 Anaplastic Large Cell Lymphoma 61 0.205
84
c SYN082 Syndromic X-Linked Intellectual Disability 14 22 0.205
85
P CRN038 Carney Complex Variant 63 0.205
86
MCC012 Mccune-Albright Syndrome 69 0.205
87
EWN003 Ewing Sarcoma 70 0.205
88
SRC014 Sarcoma 64 0.205
89
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.205
90
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 62 0.205
91
HMP005 Hemiplegia 53 0.205
92
P MGR003 Migraine with Aura 51 0.205
93
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.205
94
P DRR001 Diarrhea 55 0.205
95
CNG034 Congestive Heart Failure 69 0.205
96
P DYS154 Dystonia 64 0.205
97
P LNS003 Lens Disease 33 0.205
98
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.205
99
P HYP061 Hypertrophic Cardiomyopathy 69 0.205
100
P GRV001 Graves' Disease 54 0.205
101
ADR004 Adrenal Cortical Adenocarcinoma 38 0.205
102
CYS014 Cystadenocarcinoma 51 0.205
103
SRS001 Serous Cystadenocarcinoma 51 0.205
104
INT372 Intellectual Developmental Disorder, X-Linked, Syndromic, Lujan-Fryns Type 32 0.205
105
VRL017 Viral Hemorrhagic Fever 35 0.205
106
SPN035 Spindle Cell Sarcoma 51 0.205
107
CHR546 Chronic Mountain Sickness 43 0.205
108
CLR030 Clear Cell Renal Cell Carcinoma 54 0.205
109
HYP005 Hypokalemia 55 0.205
110
P HDC001 Headache 56 0.205
111
OVR012 Ovarian Serous Cystadenocarcinoma 55 0.205
112
48X005 48,xyyy 39 0.205
113
P HYP076 Hyperthyroidism 53 0.205
114
XLN235 X-Linked Intellectual Disability with Marfanoid Habitus 28 0.205
115
P PRD021 Periodic Paralysis 42 0.205
116
P BCK002 Beckwith-Wiedemann Syndrome 61 0.145
117
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.145
118
AGN016 Aging 54 0.145
119
c BRD010 Bardet-Biedl Syndrome 1 64 0.145
120
c FNC025 Fanconi Anemia, Complementation Group J 52 0.145
121
c MCR133 Microvascular Complications of Diabetes 4 41 0.145
122
c HYP438 Hyperaldosteronism, Familial, Type Iii 35 0.145
123
c RTN043 Retinitis Pigmentosa 13 43 0.145
124
CRB189 Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, and Sensorineural Hearing Loss 36 0.145
125
P SNS001 Sensorineural Hearing Loss 59 0.145
126
CRB004 Cerebral Artery Occlusion 46 0.145
127
ATH013 Atherosclerosis Susceptibility 63 0.145
128
P LNG032 Lung Cancer 98 0.145
129
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.145
130
ADR040 Adrenal Gland Pheochromocytoma 45 0.145
131
P FML011 Familial Adenomatous Polyposis 71 0.145
132
P ERL057 Early Infantile Epileptic Encephalopathy 61 0.145
133
P FML023 Familial Hemiplegic Migraine 53 0.145
134
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 0.145
135
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 45 0.145
136
P HNT016 Huntington Disease 73 0.145
137
P CLR023 Colorectal Cancer 100 0.145
138
P PHC003 Pheochromocytoma 70 0.145
139
c SML038 Small Cell Cancer of the Lung 69 0.145
140
c MCR113 Microvascular Complications of Diabetes 3 52 0.145
141
PRM183 Primary Aldosteronism, Seizures, and Neurologic Abnormalities 26 0.145
142
c MCR130 Microvascular Complications of Diabetes 6 41 0.145
143
c MCR120 Microvascular Complications of Diabetes 7 47 0.145
144
c MJR024 Major Affective Disorder 9 40 0.145
145
c RTN129 Retinitis Pigmentosa 49 38 0.145
146
c LFR007 Li-Fraumeni Syndrome 2 44 0.145
147
c MJR022 Major Affective Disorder 8 37 0.145
148
P LFR001 Li-Fraumeni Syndrome 73 0.145
149
P MYP006 Myopia 55 0.145
150
P MCR010 Microcephaly 59 0.145
151
NRN004 Neuroendocrine Tumor 55 0.145
152
P MLN008 Melanoma 75 0.145
153
P MLT074 Multiple Endocrine Neoplasia 58 0.145
154
ADR005 Adrenal Carcinoma 61 0.145
155
P BPL003 Bipolar Disorder 56 0.145
156
c RTN041 Retinitis Pigmentosa 11 43 0.145
157
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.145
158
P CRN300 Coronary Heart Disease 1 73 0.145
159
P NSP012 Nasopharyngeal Carcinoma 60 0.145
160
NRM005 Neuromuscular Disease 63 0.145
161
P BRT004 Bartter Disease 58 0.145
162
c BRT024 Bartter Syndrome Type 4 25 0.145
163
PLC008 Placenta Disease 49 0.145
164
P MYT002 Myotonic Dystrophy 51 0.145
165
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.145
166
LRN003 Learning Disability 49 0.145
167
PST092 Posttransplant Acute Limbic Encephalitis 29 0.145
168
GNT152 Genetic Hyperaldosteronism 8 0.145
169
THY029 Thyroid Carcinoma 54 0.145
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