Search results for aqp1

155 hits were found for aqp1

# Family MCID Name MIFTS Score
1
BLD165 Blood Group, Colton System 20 3.110
2
BRN004 Brain Edema 56 2.664
3
CRT072 Creutzfeldt-Jakob Disease 70 2.617
4
P HYD006 Hydrocephalus 66 2.617
5
ADN011 Adenoid Cystic Carcinoma 70 2.590
6
PRT036 Peritonitis 64 2.590
7
P KDN017 Kidney Cancer 60 2.590
8
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 2.147
9
INT323 Intraocular Pressure Quantitative Trait Locus 62 2.147
10
NRM001 Neuromyelitis Optica 61 2.147
11
MTN003 Motion Sickness 53 2.147
12
PLY012 Polyhydramnios 46 2.147
13
OBS004 Obstructive Hydrocephalus 46 2.147
14
LPT001 Leptospirosis 66 2.115
15
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 2.115
16
P PLY014 Polycystic Kidney Disease 62 2.115
17
P CTR002 Cataract 60 2.115
18
P HRD011 Hereditary Spherocytosis 60 2.115
19
MNR012 Meniere Disease 57 2.115
20
PLY023 Polycystic Liver Disease 57 2.115
21
ACS001 Acoustic Neuroma 56 2.115
22
NPH009 Nephrolithiasis 55 2.115
23
HMN009 Hemangioblastoma 54 2.115
24
INT075 Intracranial Hypertension 53 2.115
25
P MGR003 Migraine with Aura 52 2.115
26
OLG003 Oligohydramnios 51 2.115
27
NRM004 Neuroma 51 2.115
28
BLL004 Bullous Keratopathy 49 2.115
29
P CNG003 Congenital Dyserythropoietic Anemia 49 2.115
30
PRP007 Priapism 47 2.115
31
P INN002 Inner Ear Disease 47 2.115
32
CNT025 Central Pontine Myelinolysis 46 2.115
33
HYD003 Hydrarthrosis 31 1.571
34
P OPT006 Optic Nerve Disease 60 1.538
35
P CMM008 Communicating Hydrocephalus 45 1.538
36
c CHR579 Chiari Malformation Type Ii 44 1.538
37
P CHR342 Chiari Malformation 41 1.538
38
c ANM048 Anemia, Congenital Dyserythropoietic, Type Iv 37 1.538
39
DYS030 Dysferlinopathy 29 1.538
40
INT303 Intracranial Hypertension, Idiopathic 57 1.495
41
SPN041 Spinal Cord Disease 56 1.495
42
URN010 Urinary Tract Obstruction 55 1.495
43
HPT014 Hepatorenal Syndrome 50 1.495
44
INP001 Inappropriate Adh Syndrome 49 1.495
45
SBP004 Subependymoma 46 1.495
46
HRT015 Heritable Pulmonary Arterial Hypertension 44 1.495
47
FCH001 Fuchs' Endothelial Dystrophy 44 1.495
48
CRN045 Corneal Dystrophy and Perceptive Deafness 44 1.495
49
IDP033 Idiopathic Edema 44 1.495
50
c HYP210 Hypomagnesemia 2, Renal 43 1.495
51
P CRN026 Corneal Edema 43 1.495
52
RTN072 Retinohepatoendocrinologic Syndrome 42 1.495
53
CRB033 Cerebral Degeneration 42 1.495
54
URT031 Ureteral Disease 41 1.495
55
c ANM049 Anemia, Congenital Dyserythropoietic, Type Ib 38 1.495
56
PRP028 Peripheral Vertigo 37 1.495
57
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 37 1.495
58
c ATM105 Autoimmune Disease of Peripheral Nervous System 27 1.495
59
CRB202 Cerebrovascular Benign Neoplasm 19 1.495
60
P CLR023 Colorectal Cancer 99 0.089
61
P ADN016 Adenocarcinoma 64 0.089
62
LSH001 Leishmaniasis 63 0.089
63
PLM010 Pulmonary Edema 54 0.089
64
P KLZ004 Kala-Azar 1 41 0.089
65
P LNG032 Lung Cancer 98 0.073
66
P NRB001 Neuroblastoma 72 0.073
67
OST159 Osteogenic Sarcoma 66 0.073
68
P VSC007 Vascular Disease 63 0.073
69
P END044 Endometriosis 63 0.073
70
c GLC092 Glaucoma, Primary Open Angle 62 0.073
71
c ACT027 Acute Pancreatitis 60 0.073
72
SQM006 Squamous Cell Carcinoma 60 0.073
73
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.073
74
SYN007 Synovitis 54 0.073
75
P OPN001 Open-Angle Glaucoma 49 0.073
76
HLX001 Helix Syndrome 47 0.073
77
CRB004 Cerebral Artery Occlusion 45 0.073
78
PLC002 Plica Syndrome 36 0.073
79
P OVR042 Ovarian Cancer 88 0.052
80
P ALZ034 Alzheimer Disease 88 0.052
81
c LKM061 Leukemia, Acute Myeloid 84 0.052
82
CYS001 Cystic Fibrosis 81 0.052
83
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.052
84
P RHM011 Rheumatoid Arthritis 80 0.052
85
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.052
86
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.052
87
c MNN043 Meningioma, Familial 74 0.052
88
MSC157 Muscular Dystrophy, Duchenne Type 72 0.052
89
P SRC025 Sarcoidosis 1 70 0.052
90
DFC004 Deficiency Anemia 70 0.052
91
GST040 Gastric Adenocarcinoma 70 0.052
92
CHL065 Cholangiocarcinoma 68 0.052
93
PNC129 Pancreatic Adenocarcinoma 68 0.052
94
ALL003 Allergic Rhinitis 67 0.052
95
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.052
96
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.052
97
P MSC005 Muscular Dystrophy 66 0.052
98
P NSP012 Nasopharyngeal Carcinoma 66 0.052
99
P MCR115 Microvascular Complications of Diabetes 5 66 0.052
100
P MNN013 Meningitis 66 0.052
101
P PLM036 Pulmonary Fibrosis 65 0.052
102
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.052
103
OVR029 Ovarian Hyperstimulation Syndrome 64 0.052
104
P PRD008 Periodontitis 64 0.052
105
P HML002 Hemolytic Anemia 63 0.052
106
c ANM038 Anemia, Autoimmune Hemolytic 62 0.052
107
MNN042 Meningioma, Radiation-Induced 62 0.052
108
CTN007 Cutaneous Leishmaniasis 62 0.052
109
PSR001 Psoriatic Arthritis 61 0.052
110
ALC006 Alcoholic Hepatitis 61 0.052
111
P MYL006 Myeloid Leukemia 60 0.052
112
SPN186 Spinal Cord Injury 60 0.052
113
P BNG030 Benign Ependymoma 60 0.052
114
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 60 0.052
115
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.052
116
ISC004 Ischemia 58 0.052
117
EYD002 Eye Disease 58 0.052
118
EXT034 Extrinsic Allergic Alveolitis 58 0.052
119
BRN056 Bronchopulmonary Dysplasia 57 0.052
120
P EXN002 Exanthem 57 0.052
121
P RHN004 Rhinitis 57 0.052
122
CHR177 Chromophobe Renal Cell Carcinoma 57 0.052
123
HYP266 Hypoxia 57 0.052
124
ALL006 Allergic Asthma 56 0.052
125
ERY051 Erythroleukemia, Familial 56 0.052
126
AGN016 Aging 56 0.052
127
VSC003 Visceral Leishmaniasis 55 0.052
128
c BCT007 Bacterial Meningitis 55 0.052
129
P DBT005 Diabetes Insipidus 55 0.052
130
P LRY044 Larynx Cancer 55 0.052
131
CLL010 Cellular Ependymoma 54 0.052
132
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.052
133
OCL069 Ocular Motor Apraxia 51 0.052
134
CLR109 Colorectal Adenocarcinoma 51 0.052
135
INT079 Intrahepatic Cholangiocarcinoma 51 0.052
136
P LSS002 Lissencephaly 51 0.052
137
P AST007 Astrocytoma 51 0.052
138
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.052
139
SPN021 Spinal Meningioma 50 0.052
140
c HYD064 Hydrocephalus, Congenital, 1 48 0.052
141
c CNG216 Congenital Hydrocephalus 47 0.052
142
MYC005 Myocardial Stunning 46 0.052
143
P BNG032 Benign Mesothelioma 46 0.052
144
URT010 Ureteral Obstruction 45 0.052
145
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.052
146
DYS032 Dystrophinopathies 43 0.052
147
c MLG079 Malignant Pleural Mesothelioma 42 0.052
148
OBS082 Obstructive Nephropathy 42 0.052
149
SCR001 Secretory Meningioma 41 0.052
150
48X005 48,xyyy 39 0.052
151
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.052
152
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 33 0.052
153
QLT008 Qualitative or Quantitative Defects of Dysferlin 30 0.052
154
HML054 Hemolytic Disease Due to Fetomaternal Alloimmunization 22 0.052
155
QLT002 Qualitative or Quantitative Defects of Dystrophin 20 0.052
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