Search results for FAD

241 hits were found for FAD

# Family MCID Name MIFTS Score
1
P FTL069 Fetal Akinesia Deformation Sequence 1 55 6.012
2
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 2.717
3
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 2.717
4
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.267
5
P ALZ034 Alzheimer Disease 90 0.156
6
c FTL071 Fetal Akinesia Deformation Sequence 3 23 0.150
7
RBF001 Riboflavin Deficiency 46 0.102
8
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.093
9
P CHR012 Chronic Granulomatous Disease 69 0.093
10
P CRN018 Coronary Artery Anomaly 67 0.093
11
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.083
12
DRM006 Dermatitis 63 0.083
13
ART140 Arteries, Anomalies of 60 0.083
14
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.083
15
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.083
16
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.083
17
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.083
18
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.083
19
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.083
20
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.083
21
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.083
22
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.083
23
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.083
24
BCK006 Back Pain 44 0.083
25
ALK024 Alkuraya-Kucinskas Syndrome 41 0.083
26
CNG506 Congenital Amyoplasia 26 0.083
27
P LYM118 Lymphoma 70 0.072
28
CLF027 Cleft Palate, Isolated 67 0.072
29
IRR002 Irritable Bowel Syndrome 65 0.072
30
ETN001 Eating Disorder 61 0.072
31
PLY012 Polyhydramnios 48 0.072
32
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.059
33
c DLT002 Dilated Cardiomyopathy 81 0.059
34
c ATR087 Atrial Standstill 1 76 0.059
35
P ATS364 Autism 68 0.059
36
P DRM053 Dermatitis, Atopic 68 0.059
37
P MCR115 Microvascular Complications of Diabetes 5 67 0.059
38
P CLC063 Celiac Disease 1 66 0.059
39
CHG001 Chagas Disease 66 0.059
40
LPD008 Lipid Metabolism Disorder 64 0.059
41
P ENC018 Encephalopathy 64 0.059
42
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.059
43
P PSR002 Psoriasis 63 0.059
44
P MYP004 Myopathy 63 0.059
45
HYP066 Hyperglycemia 63 0.059
46
P ANP001 Anaplastic Large Cell Lymphoma 62 0.059
47
P CTR002 Cataract 62 0.059
48
P SCL018 Scoliosis 61 0.059
49
P MYC008 Myocarditis 60 0.059
50
IRN002 Iron Metabolism Disease 58 0.059
51
AGN016 Aging 58 0.059
52
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.059
53
CHR081 Choroideremia 54 0.059
54
PRP036 Peripheral T-Cell Lymphoma 53 0.059
55
MCL006 Macular Retinal Edema 52 0.059
56
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.059
57
PST011 Pustulosis of Palm and Sole 51 0.059
58
ATS010 Autosomal Recessive Disease 49 0.059
59
47X002 47,xyy 49 0.059
60
LYM019 Lymphosarcoma 48 0.059
61
DBT006 Diabetic Macular Edema 46 0.059
62
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.059
63
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.059
64
PRN039 Paraneoplastic Syndromes 37 0.059
65
CND006 Candida Glabrata 33 0.059
66
P CLR023 Colorectal Cancer 100 0.042
67
P BRS047 Breast Cancer 99 0.042
68
c HYP595 Hypertension, Essential 87 0.042
69
MYL069 Myeloma, Multiple 85 0.042
70
STR067 Stroke, Ischemic 82 0.042
71
P HRT032 Heart Disease 78 0.042
72
P NRF023 Neurofibromatosis, Type Ii 77 0.042
73
c CWD006 Cowden Syndrome 1 76 0.042
74
P EPL164 Epilepsy 73 0.042
75
PHN003 Phenylketonuria 73 0.042
76
P HNT016 Huntington Disease 72 0.042
77
OTT002 Otitis Media 71 0.042
78
P ART022 Arthritis 71 0.042
79
P LVR013 Liver Disease 71 0.042
80
CRB039 Cerebrovascular Disease 71 0.042
81
P HYP086 Hypothyroidism 70 0.042
82
c ATS007 Autism Spectrum Disorder 69 0.042
83
P MYC084 Mycobacterium Tuberculosis 1 69 0.042
84
LGH007 Leigh Syndrome 69 0.042
85
P MJR001 Major Depressive Disorder 69 0.042
86
P MYS003 Myasthenia Gravis 68 0.042
87
P DMN002 Dementia 68 0.042
88
HYP056 Hypoglycemia 68 0.042
89
SKN019 Skin Melanoma 68 0.042
90
MLN008 Melanoma 68 0.042
91
CRP001 Carpal Tunnel Syndrome 68 0.042
92
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 67 0.042
93
P FLL037 Follicular Lymphoma 67 0.042
94
P DBT009 Diabetes Mellitus 66 0.042
95
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.042
96
P MTR004 Maturity-Onset Diabetes of the Young 66 0.042
97
PRT037 Pertussis 66 0.042
98
P PRS038 Personality Disorder 66 0.042
99
P CWD010 Cowden Syndrome 66 0.042
100
P NRB010 Neuroblastoma 1 66 0.042
101
DSS008 Disease of Mental Health 66 0.042
102
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.042
103
ANG054 Angina Pectoris 66 0.042
104
P SPN046 Spinal Muscular Atrophy 65 0.042
105
DPR016 Depression 64 0.042
106
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.042
107
P VSC011 Vasculitis 64 0.042
108
SKN016 Skin Disease 64 0.042
109
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.042
110
ART002 Arts Syndrome 63 0.042
111
P CNG001 Congenital Myasthenic Syndrome 63 0.042
112
FTT001 Fatty Liver Disease 63 0.042
113
LNG099 Lung Disease 62 0.042
114
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 62 0.042
115
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.042
116
THY029 Thyroid Carcinoma 62 0.042
117
STT001 Status Epilepticus 61 0.042
118
P DST002 Distal Arthrogryposis 61 0.042
119
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.042
120
CHR066 Chronic Fatigue Syndrome 61 0.042
122
P MYL006 Myeloid Leukemia 61 0.042
123
APP008 Appendicitis 61 0.042
124
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.042
125
PPT005 Peptic Ulcer Disease 60 0.042
126
MNT002 Mental Depression 60 0.042
127
LPT001 Leptospirosis 60 0.042
128
END030 End Stage Renal Failure 60 0.042
129
P CRN300 Coronary Heart Disease 1 59 0.042
130
NRN004 Neuroendocrine Tumor 59 0.042
131
P BPL003 Bipolar Disorder 59 0.042
132
CNS004 Constipation 59 0.042
133
P SYP003 Syphilis 59 0.042
134
c ACT210 Acute Respiratory Distress Syndrome 59 0.042
135
URN010 Urinary Tract Obstruction 59 0.042
136
P PLY011 Polycystic Ovary Syndrome 58 0.042
137
CNT047 Contact Dermatitis 58 0.042
138
P EXN002 Exanthem 58 0.042
139
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.042
140
CHL014 Cholera 58 0.042
141
P SLP005 Sleep Disorder 58 0.042
142
P INF037 Inflammatory Bowel Disease 57 0.042
143
BCT022 Bacterial Infectious Disease 57 0.042
144
APH002 Aphasia 56 0.042
145
ALL010 Allergic Contact Dermatitis 56 0.042
146
c SVR001 Severe Acute Respiratory Syndrome 56 0.042
147
PRT038 Protein-Energy Malnutrition 56 0.042
148
AMN003 Amnestic Disorder 55 0.042
149
P VNS003 Venous Insufficiency 55 0.042
150
HYP060 Hyperinsulinism 55 0.042
151
P RST001 Restless Legs Syndrome 54 0.042
152
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.042
153
HMC014 Homocysteinemia 54 0.042
154
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.042
155
SPP010 Suppressor of Tumorigenicity 3 54 0.042
156
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 54 0.042
157
HYP014 Hyperuricemia 52 0.042
158
FDL002 Food Allergy 52 0.042
159
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.042
160
P HMC002 Homocystinuria 52 0.042
161
DNT012 Dental Caries 52 0.042
162
P CHR345 Chronic Pain 52 0.042
163
P MYT002 Myotonic Dystrophy 52 0.042
164
P MSC003 Muscular Atrophy 52 0.042
165
MCR088 Microscopic Polyangiitis 51 0.042
166
RST011 Restrictive Dermopathy, Lethal 51 0.042
167
STM007 Stomatitis 51 0.042
168
c INH020 Inherited Metabolic Disorder 51 0.042
169
HYP748 Hypertelorism 50 0.042
170
P DRM007 Dermatitis Herpetiformis 50 0.042
171
HYD012 Hydrops Fetalis 49 0.042
172
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.042
173
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 49 0.042
174
P TRM004 Trimethylaminuria 49 0.042
175
PTH002 Pathological Gambling 48 0.042
176
CHR001 Churg-Strauss Syndrome 48 0.042
177
CYS002 Cystic Lymphangioma 47 0.042
178
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.042
179
c ALZ056 Alzheimer Disease 3 47 0.042
180
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.042
181
P MYC033 Myoclonus 47 0.042
182
P MTH007 Methemoglobinemia 47 0.042
183
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.042
184
CYT002 Cytokine Deficiency 46 0.042
185
HLX001 Helix Syndrome 46 0.042
186
FLL008 Folliculitis 46 0.042
187
KWS001 Kwashiorkor 46 0.042
188
c ACT076 Acute Myocarditis 45 0.042
189
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 45 0.042
190
RSP021 Respiratory Allergy 45 0.042
191
c DRM054 Dermatitis, Atopic, 2 45 0.042
192
CYN002 Cyanosis, Transient Neonatal 45 0.042
193
MLK006 Milk Allergy 44 0.042
194
OBS082 Obstructive Nephropathy 44 0.042
195
c ATS307 Autosomal Recessive Cerebellar Ataxia 44 0.042
196
ANC002 Anca-Associated Vasculitis 43 0.042
197
ANT003 Antley-Bixler Syndrome 43 0.042
198
c PCH010 Pachyonychia Congenita 3 43 0.042
199
c MJR024 Major Affective Disorder 9 42 0.042
200
GRD001 Giardiasis 42 0.042
201
CRV045 Cervical Intraepithelial Neoplasia 41 0.042
202
ARB001 Ariboflavinosis 41 0.042
203
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.042
204
c MLT010 Multiple Personality Disorder 41 0.042
205
SPS019 Spastic Paraparesis 40 0.042
206
c 2HY001 2-Hydroxyglutaric Aciduria 40 0.042
207
URM005 Uremic Pruritus 40 0.042
208
CRN048 Craniofacial-Deafness-Hand Syndrome 39 0.042
209
c MJR022 Major Affective Disorder 8 39 0.042
210
CVT001 Cavitary Optic Disc Anomalies 39 0.042
211
c PLY105 Polycystic Ovary Syndrome 1 38 0.042
212
TBS001 Tabes Dorsalis 38 0.042
213
48X005 48,xyyy 37 0.042
214
c DRM040 Dermatitis Herpetiformis, Familial 36 0.042
215
MLR009 Miliaria 35 0.042
216
AST003 Asthenopia 34 0.042
217
SPT023 Septate Uterus 34 0.042
218
RRS014 Rare Surgical Neurologic Disease 33 0.042
219
MLR001 Miliaria Rubra 32 0.042
220
CNG538 Congenital Arthrogryposis with Anterior Horn Cell Disease 30 0.042
222
WHT017 Wheat Allergy 30 0.042
223
PTL002 Patellofemoral Pain Syndrome 30 0.042
224
c HRD146 Hereditary Methemoglobinemia 29 0.042
225
ARG004 Argyria 28 0.042
226
CNG065 Congenital Contractures 28 0.042
227
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 27 0.042
228
STN013 Stenotrophomonas Maltophilia Infection 26 0.042
229
ESN016 Eosinophilic Pustular Folliculitis 26 0.042
230
c CNG223 Congenital Methemoglobinemia 25 0.042
231
MYT026 Myotonia Atrophica 25 0.042
232
ALL012 Allergic Angiitis 25 0.042
233
ALP089 Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality 24 0.042
234
NCL007 Nuclear Gene-Encoded Leigh Syndrome 24 0.042
235
FTL016 Fetal Edema 24 0.042
236
SYP005 Syphilitic Myelopathy 22 0.042
237
LPD042 Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency 21 0.042
238
MTC166 Mitochondrial Complex I Deficiency, Nuclear Type 19 20 0.042
239
c FTL072 Fetal Akinesia Deformation Sequence 4 20 0.042
240
c PRM209 Primary Trimethylaminuria 19 0.042
241
ALP025 Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 16 0.042
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