Search results for FAD

237 hits were found for FAD

# Family MCID Name MIFTS Score
1
P FTL069 Fetal Akinesia Deformation Sequence 1 64 6.527
2
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 51 2.720
3
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 2.702
4
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.275
5
P ALZ034 Alzheimer Disease 88 0.171
6
c FTL071 Fetal Akinesia Deformation Sequence 3 28 0.149
7
RBF001 Riboflavin Deficiency 49 0.101
8
P CHR012 Chronic Granulomatous Disease 67 0.093
9
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.083
10
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.083
11
LPP008 Lipoprotein Quantitative Trait Locus 62 0.083
12
DRM006 Dermatitis 61 0.083
13
ETN001 Eating Disorder 60 0.083
14
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.083
15
ART140 Arteries, Anomalies of 52 0.083
16
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.083
17
ALK024 Alkuraya-Kucinskas Syndrome 51 0.083
18
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.083
19
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.083
20
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.083
21
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.083
22
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.083
23
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.083
24
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.083
25
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.083
26
BCK006 Back Pain 42 0.083
27
CNG506 Congenital Amyoplasia 27 0.083
28
P LYM118 Lymphoma 68 0.072
29
IRR002 Irritable Bowel Syndrome 65 0.072
30
CLF027 Cleft Palate, Isolated 64 0.072
31
HLX001 Helix Syndrome 47 0.072
32
PLY012 Polyhydramnios 46 0.072
33
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.072
34
P CLR023 Colorectal Cancer 99 0.059
35
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.059
36
c DLT002 Dilated Cardiomyopathy 79 0.059
37
P ATS364 Autism 70 0.059
38
P MYP004 Myopathy 70 0.059
39
P CLC063 Celiac Disease 1 66 0.059
40
P MCR115 Microvascular Complications of Diabetes 5 66 0.059
41
CHG001 Chagas Disease 66 0.059
42
P DRM053 Dermatitis, Atopic 66 0.059
43
LPD008 Lipid Metabolism Disorder 62 0.059
44
P PSR002 Psoriasis 62 0.059
45
P ENC018 Encephalopathy 61 0.059
46
P SCL018 Scoliosis 60 0.059
47
P CTR002 Cataract 60 0.059
48
P MYC008 Myocarditis 59 0.059
49
P ANP001 Anaplastic Large Cell Lymphoma 58 0.059
50
CHR081 Choroideremia 57 0.059
51
IRN002 Iron Metabolism Disease 57 0.059
52
AGN016 Aging 56 0.059
53
MCL006 Macular Retinal Edema 55 0.059
54
PRP036 Peripheral T-Cell Lymphoma 53 0.059
55
PST011 Pustulosis of Palm and Sole 52 0.059
56
P RCT021 Rectum Cancer 52 0.059
57
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.059
58
47X002 47,xyy 49 0.059
59
ATS010 Autosomal Recessive Disease 48 0.059
60
DBT006 Diabetic Macular Edema 48 0.059
61
LYM019 Lymphosarcoma 46 0.059
62
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.059
63
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.059
64
PRN039 Paraneoplastic Syndromes 38 0.059
65
CND006 Candida Glabrata 32 0.059
66
P BRS047 Breast Cancer 97 0.041
67
MYL069 Myeloma, Multiple 85 0.041
68
c HYP595 Hypertension, Essential 84 0.041
69
STR067 Stroke, Ischemic 81 0.041
70
c NRF023 Neurofibromatosis, Type Ii 80 0.041
71
c CWD006 Cowden Syndrome 1 78 0.041
72
P HRT032 Heart Disease 75 0.041
73
PHN003 Phenylketonuria 75 0.041
74
c ATR087 Atrial Standstill 1 75 0.041
75
P HNT016 Huntington Disease 72 0.041
76
P NRB001 Neuroblastoma 72 0.041
77
OTT002 Otitis Media 72 0.041
78
LGH007 Leigh Syndrome 70 0.041
79
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.041
80
P MLN008 Melanoma 69 0.041
81
P ART022 Arthritis 69 0.041
82
P HYP086 Hypothyroidism 69 0.041
83
P LVR013 Liver Disease 68 0.041
84
P MYC084 Mycobacterium Tuberculosis 1 68 0.041
85
SKN019 Skin Melanoma 68 0.041
86
P MYS003 Myasthenia Gravis 68 0.041
87
P MJR001 Major Depressive Disorder 68 0.041
88
P CWD010 Cowden Syndrome 67 0.041
89
P FLL037 Follicular Lymphoma 67 0.041
90
c ATS007 Autism Spectrum Disorder 67 0.041
91
CRP001 Carpal Tunnel Syndrome 67 0.041
92
LPT001 Leptospirosis 66 0.041
93
ANG054 Angina Pectoris 66 0.041
94
P DMN002 Dementia 66 0.041
95
P CNG001 Congenital Myasthenic Syndrome 66 0.041
96
HYP056 Hypoglycemia 66 0.041
97
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.041
98
P MTR004 Maturity-Onset Diabetes of the Young 65 0.041
99
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.041
100
PRT037 Pertussis 65 0.041
101
P PRS038 Personality Disorder 65 0.041
102
P DBT009 Diabetes Mellitus 64 0.041
103
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.041
104
ART002 Arts Syndrome 64 0.041
105
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.041
106
P CRN300 Coronary Heart Disease 1 63 0.041
107
P DST002 Distal Arthrogryposis 63 0.041
108
SKN016 Skin Disease 63 0.041
109
DPR016 Depression 63 0.041
110
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.041
111
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.041
112
P SPN046 Spinal Muscular Atrophy 62 0.041
113
c SVR001 Severe Acute Respiratory Syndrome 62 0.041
114
HYD038 Hydrops Fetalis, Nonimmune 62 0.041
115
P VSC011 Vasculitis 62 0.041
116
ATM095 Autoimmune Disease 62 0.041
117
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.041
119
HYP066 Hyperglycemia 61 0.041
120
FTT001 Fatty Liver Disease 61 0.041
121
CHR001 Churg-Strauss Syndrome 61 0.041
122
CHR066 Chronic Fatigue Syndrome 61 0.041
123
APP008 Appendicitis 61 0.041
124
P MYL006 Myeloid Leukemia 60 0.041
125
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.041
126
LNG099 Lung Disease 60 0.041
127
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.041
128
STT001 Status Epilepticus 60 0.041
129
CHL014 Cholera 59 0.041
130
THY029 Thyroid Carcinoma 59 0.041
131
P SLP005 Sleep Disorder 59 0.041
132
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.041
133
PPT005 Peptic Ulcer Disease 59 0.041
134
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.041
135
P SYP003 Syphilis 58 0.041
136
ISC004 Ischemia 58 0.041
137
CNT047 Contact Dermatitis 58 0.041
138
DSS008 Disease of Mental Health 58 0.041
139
MNT002 Mental Depression 58 0.041
140
CNS004 Constipation 58 0.041
141
P EXN002 Exanthem 57 0.041
142
P HDC001 Headache 57 0.041
143
c ALZ056 Alzheimer Disease 3 57 0.041
144
APH002 Aphasia 57 0.041
145
P BPL003 Bipolar Disorder 56 0.041
146
P PLY011 Polycystic Ovary Syndrome 56 0.041
147
BCT022 Bacterial Infectious Disease 56 0.041
148
ALL010 Allergic Contact Dermatitis 56 0.041
149
NRN004 Neuroendocrine Tumor 55 0.041
150
NPH009 Nephrolithiasis 55 0.041
151
P VNS003 Venous Insufficiency 55 0.041
152
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 0.041
153
P DRM007 Dermatitis Herpetiformis 55 0.041
154
URN010 Urinary Tract Obstruction 55 0.041
155
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 55 0.041
156
HYP060 Hyperinsulinism 54 0.041
157
AMN003 Amnestic Disorder 54 0.041
158
P RST001 Restless Legs Syndrome 54 0.041
159
PRT038 Protein-Energy Malnutrition 54 0.041
160
RST011 Restrictive Dermopathy, Lethal 54 0.041
161
P INF037 Inflammatory Bowel Disease 54 0.041
162
P HMC002 Homocystinuria 53 0.041
163
HMC014 Homocysteinemia 53 0.041
164
DNT012 Dental Caries 53 0.041
165
P MSC003 Muscular Atrophy 52 0.041
166
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.041
167
HYP014 Hyperuricemia 52 0.041
168
P SPP010 Suppressor of Tumorigenicity 3 51 0.041
169
MCR088 Microscopic Polyangiitis 51 0.041
170
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.041
171
FDL002 Food Allergy 51 0.041
172
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 51 0.041
173
END086 End Stage Renal Disease 51 0.041
174
DND001 Dandy-Walker Syndrome 50 0.041
175
STM007 Stomatitis 50 0.041
176
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.041
177
HYP748 Hypertelorism 50 0.041
178
P MYT002 Myotonic Dystrophy 49 0.041
179
CRN048 Craniofacial-Deafness-Hand Syndrome 49 0.041
180
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.041
181
PTH002 Pathological Gambling 49 0.041
182
CYS002 Cystic Lymphangioma 48 0.041
183
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.041
184
MLK006 Milk Allergy 48 0.041
185
c INH020 Inherited Metabolic Disorder 47 0.041
186
ANT003 Antley-Bixler Syndrome 47 0.041
187
c ACT076 Acute Myocarditis 46 0.041
188
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.041
189
P TRM004 Trimethylaminuria 46 0.041
190
FLL008 Folliculitis 46 0.041
191
P MTH007 Methemoglobinemia 46 0.041
192
P MYC033 Myoclonus 46 0.041
193
RSP021 Respiratory Allergy 45 0.041
194
CYN002 Cyanosis, Transient Neonatal 45 0.041
195
GRD001 Giardiasis 45 0.041
196
c DRM054 Dermatitis, Atopic, 2 44 0.041
197
P CHR345 Chronic Pain 44 0.041
198
c PCH010 Pachyonychia Congenita 3 44 0.041
199
KWS001 Kwashiorkor 44 0.041
200
URM005 Uremic Pruritus 42 0.041
201
CYT002 Cytokine Deficiency 42 0.041
202
P CLS010 Cluster Headache 42 0.041
203
OBS082 Obstructive Nephropathy 42 0.041
204
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.041
205
ANC002 Anca-Associated Vasculitis 41 0.041
206
c MJR024 Major Affective Disorder 9 41 0.041
207
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.041
208
CRV045 Cervical Intraepithelial Neoplasia 39 0.041
209
48X005 48,xyyy 39 0.041
210
c PLY105 Polycystic Ovary Syndrome 1 38 0.041
211
CVT001 Cavitary Optic Disc Anomalies 38 0.041
212
SPS019 Spastic Paraparesis 38 0.041
213
c FTL072 Fetal Akinesia Deformation Sequence 4 38 0.041
214
c MJR022 Major Affective Disorder 8 38 0.041
215
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.041
216
c CNG223 Congenital Methemoglobinemia 36 0.041
217
c DRM040 Dermatitis Herpetiformis, Familial 35 0.041
218
TBS001 Tabes Dorsalis 34 0.041
219
MLR009 Miliaria 34 0.041
220
MLR001 Miliaria Rubra 34 0.041
221
PPL052 Papillomatosis, Confluent and Reticulated 33 0.041
222
SPT023 Septate Uterus 33 0.041
223
CNG538 Congenital Arthrogryposis with Anterior Horn Cell Disease 32 0.041
224
WHT017 Wheat Allergy 32 0.041
225
PTL002 Patellofemoral Pain Syndrome 31 0.041
226
c MLT010 Multiple Personality Disorder 30 0.041
227
CNG065 Congenital Contractures 27 0.041
228
ARG004 Argyria 27 0.041
229
ALP089 Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality 27 0.041
230
STN013 Stenotrophomonas Maltophilia Infection 25 0.041
231
ESN016 Eosinophilic Pustular Folliculitis 25 0.041
232
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.041
233
ALL012 Allergic Angiitis 24 0.041
234
NCL007 Nuclear Gene-Encoded Leigh Syndrome 22 0.041
235
MTC166 Mitochondrial Complex I Deficiency, Nuclear Type 19 22 0.041
236
LPD042 Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency 21 0.041
237
c PRM209 Primary Trimethylaminuria 18 0.041
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