Search results for hexa

152 hits were found for hexa

# Family MCID Name MIFTS Score
1
P TYS001 Tay-Sachs Disease 69 21.747
2
c GM2006 Gm2 Gangliosidosis 45 5.004
3
P GNG009 Gangliosidosis 44 4.644
4
c TYS005 Tay-Sachs Disease, B1 Variant 16 3.426
5
SND001 Sandhoff Disease 68 3.317
6
LYS002 Lysosomal Storage Disease 52 3.266
7
P SPN046 Spinal Muscular Atrophy 62 3.204
8
P MTR014 Motor Neuron Disease 65 3.151
9
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.573
10
P MTC003 Metachromatic Leukodystrophy 70 2.573
11
c GCH015 Gaucher Disease, Type I 70 2.573
12
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 2.573
13
c MCL013 Mucolipidosis Iv 66 2.573
14
SNS003 Sensory Peripheral Neuropathy 54 2.573
15
P MCL001 Mucolipidosis 48 2.573
16
c GM2005 Gm2-Gangliosidosis, Ab Variant 51 1.896
17
c TYS006 Tay-Sachs Disease, B Variant, Adult Form 8 1.863
18
c TYS003 Tay-Sachs Disease, B Variant, Juvenile Form 7 1.863
19
c TYS004 Tay-Sachs Disease, B Variant, Infantile Form 7 1.863
20
c GM1004 Gm1-Gangliosidosis, Type I 57 1.819
21
SPH010 Sphingolipidosis 47 1.819
22
c 46X082 46,xy Sex Reversal 46 1.819
23
FML031 Female Stress Incontinence 39 1.819
24
c 46X057 46,xy Sex Reversal 8 35 1.819
25
c NPH042 Nephrolithiasis/osteoporosis, Hypophosphatemic, 2 32 1.819
26
LBM003 Lobomycosis 31 1.819
27
MCL022 Mucolipidoses 30 1.819
28
CHR043 Chronic Inflammatory Demyelinating Polyneuritis 23 1.819
29
DPH001 Diphtheria 60 0.310
30
TTN003 Tetanus 65 0.305
31
PRT037 Pertussis 65 0.287
32
P HPT021 Hepatitis 67 0.282
33
c HPT016 Hepatitis B 59 0.277
34
PLM031 Poliomyelitis 64 0.267
35
HMP009 Haemophilus Influenzae 43 0.267
36
CRN311 Coronary Ostial Stenosis or Atresia 20 0.267
37
c PRM038 Primary Agammaglobulinemia 44 0.203
38
HRW001 Hair Whorl 36 0.165
39
c HPT003 Hepatitis a 62 0.138
40
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.138
41
P OVR042 Ovarian Cancer 88 0.128
42
P INF038 Influenza 68 0.117
43
P PRP029 Porphyria 62 0.117
44
NSS002 Neisseria Meningitidis Infection 47 0.117
45
P PRP003 Porphyria Cutanea Tarda 67 0.091
46
VRL011 Viral Infectious Disease 61 0.091
47
MNN020 Meningococcal Infection 46 0.091
48
MDD018 Middle East Respiratory Syndrome 43 0.091
49
48X005 48,xyyy 39 0.091
50
HMN044 Human Immunodeficiency Virus Type 1 71 0.074
51
P PNM007 Pneumonia 68 0.074
52
P NSP012 Nasopharyngeal Carcinoma 66 0.074
53
P VSC007 Vascular Disease 63 0.074
54
MSL001 Measles 62 0.074
55
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.074
56
CHC001 Chickenpox 60 0.074
57
P RBL001 Rubella 59 0.074
58
P MMP001 Mumps 58 0.074
59
BCT022 Bacterial Infectious Disease 56 0.074
60
P MSC003 Muscular Atrophy 52 0.074
61
47X002 47,xyy 49 0.074
62
HLX001 Helix Syndrome 47 0.074
63
SPS057 Spasticity 45 0.074
64
ATX019 Ataxia with Vitamin E Deficiency 42 0.074
65
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.074
66
HND015 Hand Skill, Relative 33 0.074
67
HRP008 Herpes Simiae 25 0.074
68
NCL008 Nuclear Ribonucleic Acid 16 0.074
69
P HPT023 Hepatocellular Carcinoma 100 0.052
70
c HYP595 Hypertension, Essential 84 0.052
71
P GST053 Gastric Cancer 83 0.052
72
STR067 Stroke, Ischemic 81 0.052
73
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.052
74
CRV035 Cervical Cancer 76 0.052
75
P OST002 Osteoporosis 74 0.052
76
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.052
77
P KDN018 Kidney Disease 72 0.052
78
P NRB001 Neuroblastoma 72 0.052
79
OTT002 Otitis Media 72 0.052
80
P EPL164 Epilepsy 71 0.052
81
P MYC007 Myocardial Infarction 70 0.052
82
c CHR684 Chronic Kidney Disease 70 0.052
83
CNG034 Congestive Heart Failure 69 0.052
84
P SLP006 Sleep Apnea 69 0.052
85
LYM133 Lymphoma, Hodgkin, Classic 69 0.052
86
P FLL037 Follicular Lymphoma 67 0.052
87
SRC014 Sarcoma 65 0.052
88
P HRM001 Hermansky-Pudlak Syndrome 64 0.052
89
P PRD008 Periodontitis 64 0.052
90
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.052
91
P GLM045 Glioma 63 0.052
92
LPD008 Lipid Metabolism Disorder 62 0.052
93
P HYP750 Hypertriglyceridemia, Familial 62 0.052
94
TXC005 Toxic Shock Syndrome 62 0.052
95
HYP066 Hyperglycemia 61 0.052
96
HRP004 Herpes Zoster 60 0.052
97
ACQ007 Acquired Immunodeficiency Syndrome 60 0.052
98
INS001 Insulinoma 60 0.052
99
P THL005 Thalassemia 60 0.052
100
CHL014 Cholera 59 0.052
101
THY029 Thyroid Carcinoma 59 0.052
102
P SLP005 Sleep Disorder 59 0.052
103
VSL002 Visual Epilepsy 59 0.052
104
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.052
105
GST045 Gastroenteritis 59 0.052
106
PPT005 Peptic Ulcer Disease 59 0.052
107
P ANP001 Anaplastic Large Cell Lymphoma 58 0.052
108
ANT024 Anthrax Disease 58 0.052
109
P BCL017 B-Cell Lymphoma 58 0.052
110
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.052
111
P PRN023 Prion Disease 57 0.052
112
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.052
113
BLR008 Bilirubin Metabolic Disorder 57 0.052
114
CYT008 Cytomegalovirus Infection 57 0.052
115
P FBR017 Fibrosarcoma 56 0.052
116
P SZR006 Seizure Disorder 56 0.052
117
SBC001 Subacute Sclerosing Panencephalitis 56 0.052
118
PRP082 Porphyria, Congenital Erythropoietic 56 0.052
119
P GST044 Gastritis 56 0.052
120
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.052
121
P SLM003 Salmonellosis 55 0.052
122
HMS001 Hemosiderosis 54 0.052
123
P TRM003 Tremor 54 0.052
124
CLL003 Cellulitis 54 0.052
125
SPN035 Spindle Cell Sarcoma 53 0.052
126
P SPP010 Suppressor of Tumorigenicity 3 51 0.052
127
c HRM005 Hermansky-Pudlak Syndrome 1 51 0.052
128
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.052
129
HYP017 Hypophosphatemia 50 0.052
130
c FLL041 Follicular Lymphoma 1 49 0.052
131
ADT003 Auditory System Disease 48 0.052
132
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.052
133
P RNL015 Renal Hypertension 47 0.052
134
c JBR025 Joubert Syndrome 17 46 0.052
135
c HRM007 Hermansky-Pudlak Syndrome 4 46 0.052
136
GLL048 Glial Tumor 45 0.052
137
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.052
138
CLP005 Ciliopathy 43 0.052
139
P HYP265 Hypotonia 43 0.052
140
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.052
141
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.052
142
P RRH023 Rare Hereditary Hemochromatosis 41 0.052
143
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.052
144
OVR094 Ovarian Epithelial Cancer 38 0.052
145
ASC001 Ascaridiasis 35 0.052
146
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.052
147
DDN004 Duodenogastric Reflux 33 0.052
148
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.052
149
LYS029 Lysosomal Disease 28 0.052
150
CHL079 Children's Interstitial Lung Disease 26 0.052
151
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.052
152
PRN071 Parenteral Nutrition-Associated Cholestasis 25 0.052
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