Search results for FAD

60 hits were found for FAD

# Family MCID Name MIFTS Score
1
FTL009 Fetal Akinesia Deformation Sequence 54 4.755
2
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 57 2.671
3
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 2.618
4
NRN002 Neuronitis 43 0.142
5
P ALZ034 Alzheimer Disease 95 0.110
6
P CRN018 Coronary Artery Anomaly 69 0.110
7
ART140 Arteries, Anomalies of 51 0.110
8
P LYM118 Lymphoma 71 0.090
9
AGN016 Aging 65 0.090
10
LYM019 Lymphosarcoma 58 0.090
11
CHR081 Choroideremia 57 0.090
12
MCL006 Macular Retinal Edema 51 0.090
13
DBT006 Diabetic Macular Edema 49 0.090
14
PRP036 Peripheral T-Cell Lymphoma 48 0.090
15
RST011 Restrictive Dermopathy, Lethal 45 0.090
16
LYM024 Lymphatic System Disease 45 0.090
17
PRN039 Paraneoplastic Syndromes 35 0.090
18
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.063
19
c MCL042 Macular Degeneration, Age-Related, 1 79 0.063
20
P DLT002 Dilated Cardiomyopathy 76 0.063
21
THY028 Thyroid Cancer 72 0.063
22
P DBT009 Diabetes Mellitus 72 0.063
23
P PNM007 Pneumonia 70 0.063
24
P DRM053 Dermatitis, Atopic 68 0.063
25
SKN016 Skin Disease 68 0.063
26
P CNJ013 Conjunctivitis 67 0.063
27
DRM006 Dermatitis 67 0.063
28
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.063
29
P MTR004 Maturity-Onset Diabetes of the Young 62 0.063
30
PRS047 Prostatitis 59 0.063
31
P ENC018 Encephalopathy 58 0.063
32
P MYC008 Myocarditis 58 0.063
33
RTN018 Retinal Disease 56 0.063
34
P RTN016 Retinal Degeneration 56 0.063
35
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.063
36
P THY032 Thyroiditis 56 0.063
37
FDL002 Food Allergy 55 0.063
38
P VNS003 Venous Insufficiency 53 0.063
39
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.063
40
c PNS012 Paine Syndrome 52 0.063
41
P MYT002 Myotonic Dystrophy 50 0.063
42
ANT003 Antley-Bixler Syndrome 50 0.063
43
c ACT076 Acute Myocarditis 48 0.063
44
SKN027 Skin Conditions 48 0.063
45
P MTH007 Methemoglobinemia 46 0.063
46
MCL027 Macular Dystrophy, Dominant Cystoid 45 0.063
47
c L2H001 L-2-Hydroxyglutaric Aciduria 43 0.063
48
CRB009 Cerebritis 41 0.063
49
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 40 0.063
50
MTH064 Methemoglobinemia, Beta-Globin Type 38 0.063
51
c BLD140 Blood Group, I System 37 0.063
52
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 37 0.063
53
ART137 Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect 34 0.063
54
TBS001 Tabes Dorsalis 33 0.063
55
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.063
56
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.063
57
c CNG223 Congenital Methemoglobinemia 30 0.063
58
PTL002 Patellofemoral Pain Syndrome 30 0.063
59
c FNC024 Fanconi Anemia, Complementation Group D1 28 0.063
60
ARL004 Aural Atresia, Congenital 27 0.063
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