Search results for PIEZO1

160 hits were found for PIEZO1

# Family MCID Name MIFTS Score
1
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 47 53.974
2
c LYM149 Lymphatic Malformation 6 28 40.057
3
HRD218 Hereditary Stomatocytosis 30 22.182
4
P HML002 Hemolytic Anemia 62 22.125
6
c CNG027 Congenital Hemolytic Anemia 48 16.005
7
MLR004 Malaria 80 15.848
8
PLY012 Polyhydramnios 46 14.808
9
IMM039 Immune Hydrops Fetalis 33 13.620
10
c HMC039 Hemochromatosis, Type 1 73 12.623
11
P HRD011 Hereditary Spherocytosis 64 10.658
12
c ART119 Arthrogryposis, Distal, Type 5 51 10.574
13
P DST002 Distal Arthrogryposis 65 9.111
14
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 8.927
15
HNN001 Hennekam Syndrome 53 8.335
16
P HRD012 Hereditary Elliptocytosis 55 8.295
17
c DVL060 Developmental and Epileptic Encephalopathy 50 36 8.055
18
GLT040 Glutamate-Cysteine Ligase Deficiency 31 8.055
19
HYD038 Hydrops Fetalis, Nonimmune 59 7.781
20
P OST122 Osteogenesis Imperfecta, Type Iii 57 7.477
21
c ART120 Arthrogryposis, Distal, Type 3 49 7.477
22
CNG017 Congenital Nonspherocytic Hemolytic Anemia 33 7.477
23
P BRS047 Breast Cancer 98 4.561
24
HMS001 Hemosiderosis 48 4.441
25
GLL048 Glial Tumor 52 4.317
26
GLM045 Glioma 63 4.317
27
P RRH023 Rare Hereditary Hemochromatosis 54 4.065
28
P PNC044 Pancreatitis 61 3.409
29
DFC004 Deficiency Anemia 74 3.408
30
DGN001 Degenerative Disc Disease 49 3.349
31
P BCL017 B-Cell Lymphoma 59 3.280
32
48X005 48,xyyy 39 3.280
33
P GST053 Gastric Cancer 83 3.155
34
OST012 Osteoarthritis 77 3.059
35
BNR002 Bone Resorption Disease 47 2.898
36
P PLM037 Pulmonary Hypertension 72 2.873
37
OST159 Osteogenic Sarcoma 66 2.873
38
TRM010 Traumatic Brain Injury 51 2.637
39
P THL005 Thalassemia 56 2.630
40
P VSC007 Vascular Disease 63 2.551
41
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.462
42
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.462
43
P CYS018 Cystitis 59 2.462
44
c CHR087 Chronic Cystitis 35 2.462
45
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.462
46
HLX001 Helix Syndrome 48 2.425
47
P BLD134 Bladder Cancer 79 2.368
48
PRS129 Prostatic Hyperplasia, Benign 49 2.368
49
SRC027 Sarcoma, Synovial 58 2.368
50
P RTN024 Retinoblastoma 73 2.368
51
DSS032 Disease by Infectious Agent 55 2.368
52
SPN035 Spindle Cell Sarcoma 54 2.368
53
PRS021 Prostatic Adenoma 43 2.368
54
TXC005 Toxic Shock Syndrome 62 2.368
55
SRC014 Sarcoma 65 2.368
56
PRS045 Prostatic Hypertrophy 53 2.368
57
PLM010 Pulmonary Edema 55 2.368
58
c GLL024 Gallbladder Disease 1 52 2.269
59
BRN004 Brain Edema 54 2.269
60
P PLY018 Polycythemia 56 2.269
61
c ACT068 Acute Cystitis 61 2.269
62
BLR008 Bilirubin Metabolic Disorder 57 2.269
63
c CNG439 Congenital Lymphedema 30 2.269
64
CYT002 Cytokine Deficiency 43 2.269
65
P DBT005 Diabetes Insipidus 54 2.163
66
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.163
67
c MGR028 Migraine with or Without Aura 1 64 2.163
68
CRT069 Cortical Malformations, Occipital 30 2.163
69
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.163
70
GLB002 Glioblastoma 67 2.163
71
RTR008 Root Resorption 44 2.163
72
P ADL010 Adult Respiratory Distress Syndrome 71 2.163
73
P SCK005 Sickle Cell Disease 56 2.051
74
P PRM327 Primary Lymphedema 36 2.049
75
ORL015 Oral Squamous Cell Carcinoma 43 2.049
76
SQM006 Squamous Cell Carcinoma 60 2.049
77
P PRS040 Prostate Cancer 95 1.926
78
CRB004 Cerebral Artery Occlusion 45 1.926
79
ISC004 Ischemia 61 1.926
80
DMY004 Demyelinating Disease 50 1.926
81
SPL018 Splenomegaly 49 1.926
82
IRN004 Iron-Refractory Iron Deficiency Anemia 46 1.896
83
IRN001 Iron Deficiency Anemia 58 1.896
84
MCR018 Microcytic Anemia 47 1.896
85
IRN002 Iron Metabolism Disease 57 1.896
86
OVR093 Overhydrated Hereditary Stomatocytosis 41 1.789
87
P MYC007 Myocardial Infarction 70 1.789
88
c ACT075 Acute Myocardial Infarction 56 1.789
89
P DBT009 Diabetes Mellitus 67 1.789
90
P SCL048 Sclerosteosis 58 1.789
91
HYD005 Hydrocele 46 1.789
92
CNG506 Congenital Amyoplasia 27 1.634
93
P SCL018 Scoliosis 57 1.634
94
P MSC003 Muscular Atrophy 52 1.634
95
P NRB001 Neuroblastoma 66 1.634
96
LYM035 Lymphangiectasis 30 1.634
97
c BTT014 Beta-Thalassemia 72 1.211
98
ALL029 Allergic Disease 59 1.158
99
IRR002 Irritable Bowel Syndrome 65 1.158
100
ATH013 Atherosclerosis Susceptibility 63 1.002
101
P FML011 Familial Adenomatous Polyposis 71 1.002
102
THR024 Thrombosis 56 1.002
103
CLR108 Colorectal Adenoma 64 1.002
104
DHY015 Dehydrated Hereditary Stomatocytosis 2 23 1.002
105
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 1.002
106
VRC005 Varicose Veins 60 1.002
107
c SML038 Small Cell Cancer of the Lung 69 1.002
108
LNG039 Lung Squamous Cell Carcinoma 57 1.002
109
ADN018 Adenoma 59 1.002
110
P LNG064 Lung Cancer Susceptibility 3 70 1.002
111
P MLN008 Melanoma 76 1.002
112
MTY003 Mutyh Polyposis 30 1.002
113
BRR004 Baroreflex Failure 20 1.002
114
P KRB001 Krabbe Disease 69 0.859
115
P HNN005 Hennekam Lymphangiectasia-Lymphedema Syndrome 1 40 0.859
116
c LYM150 Lymphatic Malformation 7 38 0.859
117
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.818
118
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.818
119
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.818
120
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.818
121
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.818
122
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.818
123
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.818
124
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.818
125
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.818
126
PLC005 Placental Insufficiency 56 0.818
127
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.818
128
P ART005 Arteriovenous Malformation 65 0.818
129
MYL009 Myelodysplastic Syndrome 67 0.632
130
c MCP047 Mucopolysaccharidosis, Type Iva 62 0.579
131
STR067 Stroke, Ischemic 80 0.579
132
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.579
133
P PRK057 Parkinson Disease, Late-Onset 80 0.579
134
P ERL057 Early Infantile Epileptic Encephalopathy 60 0.579
135
HYP001 Hypochromic Microcytic Anemia 37 0.579
136
PRP036 Peripheral T-Cell Lymphoma 53 0.579
137
CRY019 Cryohydrocytosis 34 0.579
138
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.579
139
STM015 Stomatin-Deficient Cryohydrocytosis with Neurologic Defects 30 0.579
140
GMM011 Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to 25 0.579
141
c ELL005 Elliptocytosis 2 37 0.579
142
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.579
143
ANG046 Angioimmunoblastic T-Cell Lymphoma 51 0.579
144
SKN019 Skin Melanoma 71 0.579
145
P PSR002 Psoriasis 63 0.579
146
HMG002 Hemoglobinuria 50 0.579
147
P ART023 Arthropathy 61 0.579
148
MRK001 Merkel Cell Carcinoma 64 0.579
149
PST011 Pustulosis of Palm and Sole 52 0.579
150
c ELL006 Elliptocytosis 3 34 0.579
151
c ACT027 Acute Pancreatitis 60 0.579
152
P DMN001 Diamond-Blackfan Anemia 71 0.579
153
P CNG003 Congenital Dyserythropoietic Anemia 48 0.579
154
CRB039 Cerebrovascular Disease 66 0.579
155
LVR012 Liver Cirrhosis 63 0.579
156
P ENC018 Encephalopathy 62 0.579
157
P CHR345 Chronic Pain 50 0.579
158
CDC005 Cad-Cdg 6 0.579
159
P PNC035 Pancreatic Cancer 86 0.573
160
CLL010 Cellular Ependymoma 57 0.573
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