Search results for aacs

134 hits were found for aacs

# Family MCID Name MIFTS Score
1
AMP013 Ampulla of Vater Cancer 39 3.462
2
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 2.448
3
ENC044 Enchondromatosis, Multiple, Ollier Type 57 2.448
4
c SPN394 Spinal Muscular Atrophy, Type Iii 52 2.448
5
SRV001 Survival Motor Neuron Spinal Muscular Atrophy 28 2.448
6
c ATS007 Autism Spectrum Disorder 67 0.257
7
CRB037 Cerebral Palsy 68 0.252
8
P ATS364 Autism 65 0.224
9
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.218
10
APH002 Aphasia 57 0.163
11
DWN001 Down Syndrome 70 0.126
12
P THL005 Thalassemia 60 0.126
13
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.115
14
P LTR001 Lateral Sclerosis 53 0.115
15
P OVR042 Ovarian Cancer 89 0.103
16
TRM010 Traumatic Brain Injury 53 0.103
17
ACR007 Acromegaly 71 0.089
18
P ANG001 Angelman Syndrome 67 0.089
19
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.089
20
c FNC043 Fanconi Anemia, Complementation Group E 62 0.089
21
ADN018 Adenoma 58 0.089
22
CHL067 Cholecystitis 58 0.089
23
P DRR001 Diarrhea 57 0.089
25
LRN003 Learning Disability 49 0.089
26
47X002 47,xyy 49 0.089
27
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.089
28
ACL001 Acalculous Cholecystitis 35 0.089
29
STN013 Stenotrophomonas Maltophilia Infection 25 0.089
30
P ALZ034 Alzheimer Disease 88 0.073
31
P OST002 Osteoporosis 73 0.073
32
c BTT014 Beta-Thalassemia 72 0.073
33
PRP027 Peripheral Vascular Disease 71 0.073
34
CRB039 Cerebrovascular Disease 69 0.073
35
c HMP029 Hemophilia a 65 0.073
36
P DBT009 Diabetes Mellitus 64 0.073
37
P VSC007 Vascular Disease 63 0.073
38
HYP066 Hyperglycemia 61 0.073
39
GST045 Gastroenteritis 59 0.073
40
IRN002 Iron Metabolism Disease 57 0.073
41
FCT001 Factor Viii Deficiency 55 0.073
42
P HMP007 Hemophilia 51 0.073
43
APR001 Apraxia 51 0.073
44
BRN071 Brain Injury 49 0.073
45
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.073
46
SPC005 Speech Disorder 42 0.073
47
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.073
48
MYC015 Mycobacterium Fortuitum 31 0.073
49
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.073
50
FCT033 Factor Xiii, B Subunit, Deficiency of 23 0.073
51
STR067 Stroke, Ischemic 80 0.051
52
PFF001 Pfeiffer Syndrome 79 0.051
53
P BLD134 Bladder Cancer 78 0.051
54
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.051
55
c HYP836 Hypercholesterolemia, Familial, 1 72 0.051
56
RCK004 Rickets 69 0.051
57
P SLP006 Sleep Apnea 69 0.051
58
P LKM062 Leukemia, Acute Lymphoblastic 68 0.051
59
c FML021 Familial Hypercholesterolemia 68 0.051
60
P DMN002 Dementia 67 0.051
61
HYP056 Hypoglycemia 66 0.051
62
ANG054 Angina Pectoris 66 0.051
63
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 64 0.051
64
HYP020 Hyperprolactinemia 64 0.051
65
P NTR004 Neutropenia 63 0.051
66
c ACT068 Acute Cystitis 63 0.051
67
LPD008 Lipid Metabolism Disorder 62 0.051
68
c ALP101 Alpha-Thalassemia 62 0.051
69
P ERY058 Erythrocytosis, Familial, 1 61 0.051
70
c BRN108 Branchiootic Syndrome 1 61 0.051
71
DPH001 Diphtheria 60 0.051
72
DCB001 Decubitus Ulcer 60 0.051
73
P HRD011 Hereditary Spherocytosis 60 0.051
74
THY029 Thyroid Carcinoma 59 0.051
75
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.051
76
P PRV006 Pervasive Developmental Disorder 57 0.051
77
P END033 Endocarditis 57 0.051
78
P PYL005 Pyelonephritis 56 0.051
79
BCT022 Bacterial Infectious Disease 56 0.051
80
P PLY011 Polycystic Ovary Syndrome 56 0.051
81
HMG005 Hemoglobinopathy 55 0.051
82
P PLY018 Polycythemia 55 0.051
83
CHL014 Cholera 55 0.051
84
NRN004 Neuroendocrine Tumor 55 0.051
85
P MLT074 Multiple Endocrine Neoplasia 55 0.051
86
P LYM031 Lymphocytic Leukemia 55 0.051
87
P SLM003 Salmonellosis 54 0.051
88
HMS001 Hemosiderosis 54 0.051
89
c ACT020 Acute T Cell Leukemia 53 0.051
90
FCT005 Factor Xiii Deficiency 53 0.051
91
PRP080 Peripheral Artery Disease 53 0.051
92
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.051
93
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.051
94
c GLL024 Gallbladder Disease 1 52 0.051
95
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.051
96
c PRM012 Primary Polycythemia 52 0.051
97
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.051
98
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.051
99
STM007 Stomatitis 49 0.051
100
CHL004 Cholelithiasis 49 0.051
101
BCT004 Bacteriuria 48 0.051
102
HYP043 Hyperandrogenism 48 0.051
103
SPL018 Splenomegaly 48 0.051
104
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.051
105
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.051
106
HLX001 Helix Syndrome 47 0.051
107
SPC010 Speech and Communication Disorders 47 0.051
108
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.051
109
MLT006 Multidrug-Resistant Tuberculosis 47 0.051
110
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.051
111
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.051
112
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.051
113
HDN002 Head Injury 45 0.051
114
CYN002 Cyanosis, Transient Neonatal 45 0.051
115
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.051
116
MTS001 Mutism 45 0.051
117
CHL109 Childhood Apraxia of Speech 44 0.051
118
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.051
119
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.051
120
P RRH023 Rare Hereditary Hemochromatosis 41 0.051
121
P RRT020 Rare Tumor 41 0.051
122
P DYS005 Dyslexia 40 0.051
123
48X005 48,xyyy 39 0.051
124
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.051
125
OVR094 Ovarian Epithelial Cancer 38 0.051
126
c ELL005 Elliptocytosis 2 36 0.051
127
SCR003 Secretory Diarrhea 36 0.051
128
c MCR312 Microphthalmia, Syndromic 10 34 0.051
129
GLN002 Glanders 33 0.051
130
c ELL006 Elliptocytosis 3 33 0.051
131
RRS014 Rare Surgical Neurologic Disease 32 0.051
132
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.051
133
GST111 Gastroenteropancreatic Neuroendocrine Neoplasm 21 0.051
134
ERY007 Erythropoietin Polycythemia 15 0.051
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