Search results for ina

107 hits were found for ina

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 88 3.528
2
P MTR014 Motor Neuron Disease 64 3.528
3
GLM004 Gliomatosis Cerebri 52 2.916
4
P FRN006 Frontotemporal Dementia 70 2.880
5
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 61 2.880
6
WRN003 Wernicke Encephalopathy 47 2.880
7
MDL002 Medulloepithelioma 43 2.880
8
PCK003 Pick Disease of Brain 68 2.037
9
SPN028 Spondyloepimetaphyseal Dysplasia, Strudwick Type 51 2.037
10
P OTS002 Otospondylomegaepiphyseal Dysplasia 46 2.037
11
HYP231 Hypothalamic Hamartomas 46 2.037
12
c RTN090 Retinitis Pigmentosa 55 41 2.037
13
NDL005 Nodular Medulloblastoma 40 2.037
14
MDL003 Medullomyoblastoma 32 2.037
15
GST111 Gastroenteropancreatic Neuroendocrine Neoplasm 21 2.037
16
P OVR082 Overgrowth Syndrome 50 0.205
17
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.170
18
P BRG001 Brugada Syndrome 70 0.098
19
c THR092 Thrombophilia Due to Thrombin Defect 73 0.080
20
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.080
21
P ATR011 Atrial Fibrillation 66 0.080
22
P LNG028 Long Qt Syndrome 65 0.080
23
CRD223 Cardiac Arrhythmia 60 0.080
24
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.080
25
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.080
26
P CLR023 Colorectal Cancer 98 0.057
27
P BRS047 Breast Cancer 96 0.057
28
P PNC035 Pancreatic Cancer 84 0.057
29
STR067 Stroke, Ischemic 80 0.057
30
P NRF023 Neurofibromatosis, Type Ii 76 0.057
31
P OST002 Osteoporosis 73 0.057
32
P MLT020 Multiple Sclerosis 72 0.057
33
P CNR004 Cone-Rod Dystrophy 2 71 0.057
34
P NRB001 Neuroblastoma 71 0.057
35
HMN044 Human Immunodeficiency Virus Type 1 71 0.057
36
P MYC007 Myocardial Infarction 70 0.057
37
DWN001 Down Syndrome 70 0.057
38
PLM001 Pulmonary Tuberculosis 70 0.057
39
CRB039 Cerebrovascular Disease 69 0.057
40
P MYC084 Mycobacterium Tuberculosis 1 68 0.057
41
CRB037 Cerebral Palsy 68 0.057
42
PNC129 Pancreatic Adenocarcinoma 67 0.057
43
P NSP012 Nasopharyngeal Carcinoma 67 0.057
44
LPT001 Leptospirosis 66 0.057
45
c MCR129 Microvascular Complications of Diabetes 1 66 0.057
46
P NRV007 Nervous System Disease 66 0.057
47
c RHB024 Rhabdomyosarcoma 2 65 0.057
48
P TRN020 Turner Syndrome 65 0.057
49
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.057
50
NRF007 Neurofibroma 64 0.057
51
TBC004 Tobacco Addiction 64 0.057
52
GT001 Gout 63 0.057
53
P NTR004 Neutropenia 63 0.057
54
P PSR002 Psoriasis 62 0.057
55
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.057
56
CRC021 Carcinosarcoma 61 0.057
57
P ENC004 Encephalitis 61 0.057
58
BRC012 Brucellosis 61 0.057
59
c PNS012 Paine Syndrome 61 0.057
60
ISC004 Ischemia 60 0.057
61
SPN186 Spinal Cord Injury 60 0.057
62
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.057
63
TRG002 Trigeminal Neuralgia 60 0.057
64
THY029 Thyroid Carcinoma 59 0.057
65
PLM033 Pulmonary Embolism 59 0.057
66
CRD132 Cardiac Conduction Defect 59 0.057
67
CMP010 Complex Regional Pain Syndrome 58 0.057
68
QFV001 Q Fever 58 0.057
69
P CND004 Candidiasis 57 0.057
70
P DNG005 Dengue Virus 57 0.057
71
P HDC001 Headache 57 0.057
72
P PRP019 Peripheral Nervous System Disease 57 0.057
73
P GLM007 Glomerulonephritis 57 0.057
74
P STR020 Strabismus 56 0.057
75
P NRP001 Neuropathy 56 0.057
76
THR024 Thrombosis 56 0.057
77
c ACT075 Acute Myocardial Infarction 56 0.057
78
ORL005 Oral Candidiasis 56 0.057
79
CMR002 Coumarin Resistance 56 0.057
80
P SCK002 Sick Sinus Syndrome 55 0.057
81
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.057
82
DBT010 Diabetic Neuropathy 55 0.057
83
P ART021 Arteriosclerosis 54 0.057
84
HMS001 Hemosiderosis 54 0.057
85
PNC001 Pancytopenia 54 0.057
86
PRC013 Pericarditis 54 0.057
87
RFL001 Reflex Sympathetic Dystrophy 53 0.057
88
SNS003 Sensory Peripheral Neuropathy 53 0.057
89
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 53 0.057
90
PST011 Pustulosis of Palm and Sole 52 0.057
91
PYD002 Pyoderma 51 0.057
92
P MMB011 Membranous Nephropathy 50 0.057
93
P MYT002 Myotonic Dystrophy 49 0.057
94
SNT005 Sinoatrial Node Disease 49 0.057
95
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.057
96
P THY054 Thyrotoxic Periodic Paralysis 47 0.057
97
VNZ002 Venezuelan Equine Encephalitis 46 0.057
98
P PRD021 Periodic Paralysis 46 0.057
99
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.057
100
PST053 Postherpetic Neuralgia 42 0.057
101
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.057
102
P RRT020 Rare Tumor 41 0.057
103
MCH006 Mechanical Strabismus 39 0.057
104
48X005 48,xyyy 39 0.057
105
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.057
106
HMM004 Hamamy Syndrome 37 0.057
107
c CNT068 Central Pain Syndrome 29 0.057
Content
Loading form....