Search results for aaas

106 hits were found for aaas

# Family MCID Name MIFTS Score
1
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 50 22.541
2
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 13.357
3
ACH005 Achalasia 52 6.757
4
ART016 Aortic Aneurysm 70 4.650
5
ART017 Aortic Disease 57 3.821
6
ESP023 Esophageal Disease 58 3.205
7
IDP035 Idiopathic Achalasia 47 3.205
8
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 52 3.168
9
P CMP008 Compartment Syndrome 48 3.168
10
ART140 Arteries, Anomalies of 51 2.288
11
ANR040 Aneurysm 61 0.473
12
VSC007 Vascular Disease 71 0.382
13
ISC004 Ischemia 66 0.151
14
PRP016 Paraplegia 53 0.151
15
SPS057 Spasticity 41 0.151
16
c HRD010 Hereditary Spastic Paraplegia 68 0.127
17
P MYC007 Myocardial Infarction 81 0.099
18
P DBT009 Diabetes Mellitus 72 0.099
19
P NRP001 Neuropathy 63 0.099
20
THR024 Thrombosis 61 0.099
21
P DYS154 Dystonia 61 0.099
22
BNF002 Bone Fracture 56 0.099
23
HRS011 Horseshoe Kidney 35 0.099
24
P BRS047 Breast Cancer 100 0.081
25
CNG034 Congestive Heart Failure 74 0.081
26
P ADN016 Adenocarcinoma 71 0.081
27
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.081
28
ATM095 Autoimmune Disease 66 0.081
29
HYP056 Hypoglycemia 62 0.081
30
IMM136 Immune System Disease 57 0.081
31
P MYP006 Myopia 56 0.081
32
P THY032 Thyroiditis 56 0.081
33
GLC008 Glucose Metabolism Disease 38 0.081
34
c BLD140 Blood Group, I System 37 0.081
35
HYP745 Hyperreflexia 36 0.081
36
SPS019 Spastic Paraparesis 33 0.081
37
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.081
38
DYT002 Dyt1 Early-Onset Isolated Dystonia 10 0.081
39
P ALZ034 Alzheimer Disease 95 0.057
40
P PRS040 Prostate Cancer 88 0.057
41
CYS001 Cystic Fibrosis 85 0.057
42
P HRT032 Heart Disease 80 0.057
43
P INF038 Influenza 77 0.057
44
P NRV007 Nervous System Disease 75 0.057
45
GLB002 Glioblastoma 74 0.057
46
APL001 Aplastic Anemia 74 0.057
47
ISC006 Ischemic Heart Disease 73 0.057
48
PSY004 Psychotic Disorder 72 0.057
49
P CRV035 Cervical Cancer 72 0.057
50
ANX010 Anxiety 72 0.057
51
P RSP003 Respiratory Failure 71 0.057
52
BRC012 Brucellosis 71 0.057
53
WRN001 Werner Syndrome 70 0.057
54
P EPL164 Epilepsy 70 0.057
55
P KDN018 Kidney Disease 69 0.057
56
P MYC084 Mycobacterium Tuberculosis 1 69 0.057
57
P CRN018 Coronary Artery Anomaly 69 0.057
58
DMN002 Dementia 68 0.057
59
GST050 Gastrointestinal System Disease 66 0.057
60
P THL005 Thalassemia 65 0.057
61
c CNT035 Central Nervous System Disease 65 0.057
62
AGN016 Aging 65 0.057
63
HYP066 Hyperglycemia 64 0.057
64
GST092 Gastroesophageal Reflux 64 0.057
65
P PNC044 Pancreatitis 64 0.057
66
P ART021 Arteriosclerosis 62 0.057
67
HYP266 Hypoxia 61 0.057
68
P INF032 Infertility 59 0.057
69
PRS047 Prostatitis 59 0.057
70
P ENC018 Encephalopathy 58 0.057
71
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.057
72
URN009 Urinary System Disease 58 0.057
73
GLC003 Glucose Intolerance 58 0.057
74
P NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 57 0.057
75
P CRN300 Coronary Heart Disease 1 57 0.057
76
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.057
77
CHL014 Cholera 56 0.057
78
SPS003 Spastic Diplegia 55 0.057
79
c ACT071 Acute Kidney Failure 54 0.057
80
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.057
81
OPT006 Optic Nerve Disease 53 0.057
82
P CRD132 Cardiac Conduction Defect 53 0.057
83
P DYS026 Dysfibrinogenemia 51 0.057
84
P MYM013 Moyamoya Disease 1 50 0.057
85
P CRV039 Cervicitis 49 0.057
86
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.057
87
ISC002 Ischemic Optic Neuropathy 48 0.057
88
DYS073 Dysphagia 47 0.057
89
P DYS021 Dysautonomia 47 0.057
90
ESN002 Eosinophilia-Myalgia Syndrome 46 0.057
91
CRN031 Cranial Nerve Disease 45 0.057
92
HPT070 Hepatosplenic T-Cell Lymphoma 43 0.057
93
MGS001 Megaesophagus 42 0.057
94
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.057
95
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.057
96
MYC033 Myoclonus 40 0.057
97
P CRB059 Cerebellar Degeneration 40 0.057
98
DYS011 Dyskinesia of Esophagus 39 0.057
99
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.057
100
P AXN001 Axonal Neuropathy 38 0.057
101
SWL001 Swallowing Disorders 36 0.057
102
CDS002 Codas Syndrome 32 0.057
103
BJR001 Bjornstad Syndrome 32 0.057
104
P SPS008 Spastic Ataxia 32 0.057
105
ARL004 Aural Atresia, Congenital 27 0.057
106
c SPS021 Spastic Paraplegia 10 26 0.057
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