Search results for aaas

115 hits were found for aaas

# Family MCID Name MIFTS Score
1
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 49 24.313
2
c ART138 Aortic Aneurysm, Familial Abdominal, 1 64 13.434
3
ACH005 Achalasia 51 6.870
4
ART017 Aortic Disease 56 3.863
5
SPS019 Spastic Paraparesis 35 3.337
6
ESP023 Esophageal Disease 56 3.257
7
IDP035 Idiopathic Achalasia 48 3.257
8
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 54 3.222
9
ART140 Arteries, Anomalies of 65 2.324
10
ANR040 Aneurysm 60 0.485
11
ART016 Aortic Aneurysm 69 0.479
12
VSC007 Vascular Disease 68 0.375
13
TYP041 Type I 56 0.199
14
ISC004 Ischemia 65 0.192
15
P MYC007 Myocardial Infarction 79 0.166
16
PRP016 Paraplegia 53 0.156
17
SPS057 Spasticity 41 0.146
18
THR024 Thrombosis 61 0.135
19
c HRD010 Hereditary Spastic Paraplegia 67 0.124
20
BNF002 Bone Fracture 55 0.111
21
CNG034 Congestive Heart Failure 72 0.096
22
P RSP003 Respiratory Failure 70 0.096
23
P DYS154 Dystonia 64 0.096
24
P NRP001 Neuropathy 63 0.096
25
HYP056 Hypoglycemia 62 0.096
26
HRS011 Horseshoe Kidney 34 0.096
27
P LNG064 Lung Cancer Susceptibility 3 76 0.078
28
ISC006 Ischemic Heart Disease 72 0.078
29
P ADN016 Adenocarcinoma 70 0.078
30
P CRN018 Coronary Artery Anomaly 68 0.078
31
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 0.078
32
c CRN300 Coronary Heart Disease 1 64 0.078
33
ATM095 Autoimmune Disease 64 0.078
34
P DBT009 Diabetes Mellitus 64 0.078
35
AGN016 Aging 64 0.078
36
IMM136 Immune System Disease 56 0.078
37
P MYP006 Myopia 56 0.078
38
P THY032 Thyroiditis 55 0.078
39
GLC008 Glucose Metabolism Disease 52 0.078
40
ESN002 Eosinophilia-Myalgia Syndrome 45 0.078
41
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.078
42
DYT002 Dyt1 Early-Onset Isolated Dystonia 12 0.078
43
P BRS047 Breast Cancer 100 0.055
44
P PRS040 Prostate Cancer 90 0.055
45
P ALZ034 Alzheimer Disease 87 0.055
46
CYS001 Cystic Fibrosis 84 0.055
47
P RHM011 Rheumatoid Arthritis 80 0.055
48
P ART022 Arthritis 76 0.055
49
P INF038 Influenza 76 0.055
50
P HRT032 Heart Disease 74 0.055
51
P NRV007 Nervous System Disease 73 0.055
52
APL001 Aplastic Anemia 73 0.055
53
GLB002 Glioblastoma 72 0.055
54
ANX010 Anxiety 72 0.055
55
PSY004 Psychotic Disorder 71 0.055
56
BRC012 Brucellosis 70 0.055
57
P PNM007 Pneumonia 69 0.055
58
P CRV035 Cervical Cancer 69 0.055
59
WRN001 Werner Syndrome 69 0.055
60
P EPL164 Epilepsy 69 0.055
61
P HYD006 Hydrocephalus 69 0.055
62
P KDN018 Kidney Disease 68 0.055
63
DMN002 Dementia 68 0.055
64
c THR092 Thrombophilia Due to Thrombin Defect 67 0.055
65
GST050 Gastrointestinal System Disease 64 0.055
66
P THL005 Thalassemia 64 0.055
67
P PNC044 Pancreatitis 64 0.055
68
GST092 Gastroesophageal Reflux 64 0.055
69
c CNT035 Central Nervous System Disease 63 0.055
70
HYP066 Hyperglycemia 63 0.055
71
PLM033 Pulmonary Embolism 62 0.055
72
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.055
73
P ENC018 Encephalopathy 62 0.055
74
CRD119 Cardiac Arrest 62 0.055
75
P SLV002 Salivary Gland Cancer 61 0.055
76
HYP266 Hypoxia 61 0.055
77
PPT005 Peptic Ulcer Disease 61 0.055
78
DFC004 Deficiency Anemia 61 0.055
79
P ART021 Arteriosclerosis 60 0.055
80
PRS047 Prostatitis 60 0.055
81
P INF032 Infertility 59 0.055
82
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.055
83
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 59 0.055
84
P CRD132 Cardiac Conduction Defect 59 0.055
85
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.055
86
OPT006 Optic Nerve Disease 57 0.055
87
P DRR001 Diarrhea 56 0.055
88
GLC003 Glucose Intolerance 56 0.055
89
CHL014 Cholera 56 0.055
90
P INT070 Intestinal Obstruction 56 0.055
91
URN009 Urinary System Disease 55 0.055
92
IRN002 Iron Metabolism Disease 55 0.055
93
IRN001 Iron Deficiency Anemia 55 0.055
94
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.055
95
SPS003 Spastic Diplegia 54 0.055
96
c ACT071 Acute Kidney Failure 54 0.055
97
P MYM013 Moyamoya Disease 1 51 0.055
98
P DYS026 Dysfibrinogenemia 50 0.055
99
P CRV039 Cervicitis 49 0.055
100
ISC002 Ischemic Optic Neuropathy 47 0.055
101
MGS001 Megaesophagus 46 0.055
102
DYS073 Dysphagia 46 0.055
103
CRN031 Cranial Nerve Disease 45 0.055
104
P DYS021 Dysautonomia 43 0.055
105
HPT070 Hepatosplenic T-Cell Lymphoma 43 0.055
106
MYC033 Myoclonus 41 0.055
107
P CRB059 Cerebellar Degeneration 39 0.055
108
DYS011 Dyskinesia of Esophagus 39 0.055
109
P AXN001 Axonal Neuropathy 38 0.055
110
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 38 0.055
111
SWL001 Swallowing Disorders 36 0.055
112
P SPS008 Spastic Ataxia 33 0.055
113
BJR001 Bjornstad Syndrome 32 0.055
114
CDS002 Codas Syndrome 32 0.055
115
c SPS021 Spastic Paraplegia 10 26 0.055
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