Search results for "fanconi anemia, complementation group m"

The MalaCard for "fanconi anemia, complementation group m" has been retired.
Searching MalaCards for entries containing "fanconi anemia, complementation group m"

133 hits were found for 'fanconi anemia, complementation group m'

# Family MCID Name MIFTS Score
1
P LKM002 Leukemia 70 0.445
2
c FNC027 Fanconi Anemia, Complementation Group a 71 0.370
3
P HPT021 Hepatitis 74 0.314
4
P BRS047 Breast Cancer 100 0.288
5
P LYM118 Lymphoma 68 0.283
6
P LNG032 Lung Cancer 92 0.224
7
P MYL006 Myeloid Leukemia 67 0.220
8
P MYL007 Myeloma 52 0.212
9
MYL009 Myelodysplastic Syndrome 73 0.211
10
P URF003 Urofacial Syndrome 1 51 0.195
11
NTR005 Nutritional Deficiency Disease 51 0.192
12
P GLM007 Glomerulonephritis 56 0.192
13
SPN041 Spinal Cord Disease 50 0.186
14
P KDN018 Kidney Disease 64 0.185
15
P PNM007 Pneumonia 67 0.183
16
RTN023 Retinitis 49 0.179
17
c CHR090 Chronic Lymphocytic Leukemia 73 0.175
18
P ADN016 Adenocarcinoma 69 0.169
19
HMT018 Hematopoietic Stem Cell Transplantation 39 0.169
20
MLN008 Melanoma 61 0.169
21
c MLT019 Multiple Myeloma 77 0.168
22
RFR010 Refractory Anemia 43 0.166
23
P PNC044 Pancreatitis 62 0.164
24
SRC014 Sarcoma 66 0.163
25
P KDN017 Kidney Cancer 67 0.162
26
c ACT073 Acute Leukemia 61 0.162
27
BNM001 Bone Marrow Cancer 56 0.161
28
P LYM026 Lymphoblastic Leukemia 60 0.158
29
P ATX004 Ataxia 53 0.158
30
ALR002 Al-Raqad Syndrome 36 0.157
31
HPT023 Hepatocellular Carcinoma 90 0.156
32
P THY032 Thyroiditis 57 0.155
33
HV1006 Hiv-1 80 0.151
34
P CLR023 Colorectal Cancer 96 0.151
35
P OVR042 Ovarian Cancer 73 0.150
36
c INH020 Inherited Metabolic Disorder 49 0.148
37
P INF038 Influenza 71 0.143
38
c CHR089 Chronic Kidney Failure 67 0.138
39
P NRB001 Neuroblastoma 70 0.138
40
SPT005 Spotted Fever 56 0.138
41
c HPT016 Hepatitis B 61 0.136
42
c CNG401 Congenital Heart Disease 67 0.136
43
P ATX030 Ataxia-Telangiectasia 78 0.135
44
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.134
45
c CHR418 Chronic Leukemia 48 0.132
46
PCK002 Pick Disease 66 0.131
47
CSY001 C Syndrome 49 0.130
48
P MYP004 Myopathy 67 0.129
49
P PNC035 Pancreatic Cancer 86 0.128
50
P RNL014 Renal Cell Carcinoma 80 0.125
51
P CRV039 Cervicitis 45 0.124
52
URN009 Urinary System Disease 52 0.123
53
P AST005 Asthma 80 0.121
54
P TCL004 T-Cell Leukemia 44 0.119
55
MSL001 Measles 61 0.119
56
c LKM061 Leukemia, Acute Myeloid 71 0.118
57
IMP003 Impaired Renal Function Disease 36 0.118
58
BLD053 Blood Platelet Disease 44 0.118
59
P GLM045 Glioma 53 0.117
60
IMM127 Immune System Cancer 41 0.116
61
BLD054 Blood Protein Disease 38 0.115
62
END030 End Stage Renal Failure 53 0.114
63
c ADL017 Adult T-Cell Leukemia 59 0.112
64
HYP266 Hypoxia 55 0.110
65
P ESP024 Esophagitis 62 0.109
66
P PSR002 Psoriasis 63 0.109
67
P UVT001 Uveitis 60 0.107
68
P PRM006 Primary Biliary Cirrhosis 55 0.107
69
ADL002 Adult Syndrome 53 0.106
70
P FLL037 Follicular Lymphoma 68 0.104
71
P MMB011 Membranous Nephropathy 53 0.104
72
INC022 Inclusion-Cell Disease 46 0.104
73
LKC003 Leukocyte Disease 45 0.100
74
P HRP006 Herpes Simplex 65 0.100
75
RHM027 Rheumatic Disease 55 0.100
76
ACQ007 Acquired Immunodeficiency Syndrome 60 0.099
77
P PRD008 Periodontitis 46 0.099
78
GDS001 Good Syndrome 46 0.099
79
ACR041 Acromelic Frontonasal Dysostosis 45 0.098
80
WLL006 Wells Syndrome 57 0.098
81
SXL003 Sexual Disorder 45 0.098
82
SKN016 Skin Disease 69 0.097
83
BRT030 Birth Defects 44 0.096
84
PRM025 Primary Bacterial Infectious Disease 42 0.096
85
P MDL005 Medulloblastoma 76 0.095
86
ALN001 Aland Island Eye Disease 45 0.094
87
BCT015 Bacteremia 50 0.093
88
c RNL016 Renal Infectious Disease 22 0.093
89
P EPL164 Epilepsy 60 0.091
90
P INF032 Infertility 61 0.088
91
PRP027 Peripheral Vascular Disease 69 0.088
92
CRV038 Cervical Squamous Cell Carcinoma 58 0.087
93
P CLC005 Celiac Disease 67 0.086
94
MLD001 Melioidosis 67 0.085
95
P NPH012 Nephrotic Syndrome 55 0.084
96
QFV001 Q Fever 62 0.084
97
DWN001 Down Syndrome 65 0.083
98
DNG002 Dengue Hemorrhagic Fever 60 0.082
99
LVR012 Liver Cirrhosis 71 0.082
100
ACD009 Acid-Labile Subunit, Deficiency of 37 0.081
101
c ACT071 Acute Kidney Failure 48 0.080
102
c CRN214 Coronary Heart Disease 5 22 0.079
103
P BLD051 Blood Coagulation Disease 44 0.079
104
ORL011 Oral Cancer 53 0.078
105
DNG003 Dengue Disease 60 0.078
106
CNN005 Connective Tissue Disease 60 0.077
107
ADN018 Adenoma 59 0.076
108
c CLL013 Cell Type Cancer 46 0.076
109
STM007 Stomatitis 50 0.074
110
P SKN013 Skin Benign Neoplasm 38 0.074
111
URM002 Uremia 36 0.074
112
RNL101 Renal Cell Carcinoma, Papillary 63 0.073
113
ALL026 Allergic Hypersensitivity Disease 53 0.073
114
P MNC007 Monocytic Leukemia 52 0.070
115
STL001 St. Louis Encephalitis 46 0.070
116
P EXN002 Exanthem 57 0.070
117
KRT004 Keratitis 70 0.070
118
EXF001 Exfoliation Syndrome 56 0.069
119
c BSL007 Basal Cell Carcinoma 66 0.069
120
P PLN008 Peeling Skin Syndrome 45 0.068
121
SPN051 Spondylitis 50 0.068
122
SKN027 Skin Conditions 44 0.067
123
ADL030 Adult-Onset Still's Disease 57 0.066
124
c PLN018 Peeling Skin Syndrome 2 36 0.066
125
WST001 West Syndrome 61 0.063
126
THY028 Thyroid Cancer 71 0.062
127
P MCR010 Microcephaly 60 0.060
128
P LNG064 Lung Cancer Susceptibility 3 62 0.058
129
ORL015 Oral Squamous Cell Carcinoma 55 0.058
130
NRT004 Neuritis 52 0.056
131
MCR013 Microphthalmia 57 0.055
132
P ESN008 Eosinophilic Pneumonia 47 0.053
133
c ACT009 Acute Monocytic Leukemia 46 0.052