Search results for fanconi anemia, complementation group m

163 hits were found for fanconi anemia, complementation group m

# Family MCID Name MIFTS Score
1
P FNC027 Fanconi Anemia, Complementation Group a 78 0.663
2
P LKM002 Leukemia 75 0.464
3
c BLD140 Blood Group, I System 37 0.364
4
P HPT021 Hepatitis 75 0.324
5
AGN016 Aging 65 0.308
6
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.308
7
P KDN018 Kidney Disease 69 0.305
8
P BRS047 Breast Cancer 100 0.305
9
P LYM118 Lymphoma 71 0.300
10
URN009 Urinary System Disease 58 0.277
11
MYL009 Myelodysplastic Syndrome 75 0.243
12
P MYL006 Myeloid Leukemia 69 0.241
13
P LNG032 Lung Cancer 99 0.235
14
SQM006 Squamous Cell Carcinoma 74 0.227
15
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.226
16
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.223
17
P DBT009 Diabetes Mellitus 72 0.218
18
c LKM061 Leukemia, Acute Myeloid 81 0.214
19
MYL069 Myeloma, Multiple 86 0.190
20
P ADN016 Adenocarcinoma 71 0.189
21
c CHR089 Chronic Kidney Failure 72 0.188
22
MLN008 Melanoma 72 0.186
23
HMT018 Hematopoietic Stem Cell Transplantation 58 0.182
24
P PNM007 Pneumonia 70 0.180
25
P RNG031 Ring Chromosome Y Syndrome 29 0.180
26
RFR010 Refractory Anemia 48 0.176
27
P LYM026 Lymphoblastic Leukemia 66 0.176
28
SRC014 Sarcoma 68 0.175
29
ALP046 Alport Syndrome, X-Linked 74 0.174
30
P MGL001 Megaloblastic Anemia 52 0.174
31
c HPT001 Hepatitis C 73 0.172
32
P MYC084 Mycobacterium Tuberculosis 1 69 0.171
33
ACQ007 Acquired Immunodeficiency Syndrome 65 0.171
34
P PNC044 Pancreatitis 64 0.169
35
P CLR023 Colorectal Cancer 98 0.169
36
P GLM007 Glomerulonephritis 61 0.168
37
P ANR048 Aniridia 1 68 0.168
38
BLD137 Blood Group--Ahonen 17 0.168
39
ANR038 Anorexia Nervosa 1 21 0.167
40
P HPT023 Hepatocellular Carcinoma 94 0.166
41
RTN023 Retinitis 52 0.164
42
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.161
43
P OVR042 Ovarian Cancer 82 0.156
44
c LKM071 Leukemia, Chronic Lymphocytic 75 0.156
45
P THY032 Thyroiditis 56 0.153
46
c HPT016 Hepatitis B 68 0.151
47
THR024 Thrombosis 61 0.149
48
ALR002 Al-Raqad Syndrome 30 0.147
49
AST005 Asthma 83 0.144
50
P FNC043 Fanconi Anemia, Complementation Group E 52 0.143
51
P BCL006 B-Cell Lymphomas 70 0.140
52
P LVR013 Liver Disease 76 0.139
53
LYM019 Lymphosarcoma 58 0.139
54
c SML038 Small Cell Cancer of the Lung 67 0.138
55
P INF038 Influenza 77 0.137
56
ACT118 Acute Non Lymphoblastic Leukemia 32 0.136
57
P CRV039 Cervicitis 49 0.136
58
P NRB001 Neuroblastoma 73 0.136
59
P ATX030 Ataxia-Telangiectasia 80 0.135
60
P THR014 Thrombocytopenia 65 0.134
61
P PNC035 Pancreatic Cancer 89 0.134
62
END030 End Stage Renal Failure 59 0.134
63
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.132
64
P MYP004 Myopathy 69 0.131
65
HYP266 Hypoxia 61 0.131
66
LYM024 Lymphatic System Disease 45 0.128
67
c ACT073 Acute Leukemia 61 0.127
68
c LKM004 Leukemia, B-Cell, Chronic 37 0.127
69
P ENC018 Encephalopathy 58 0.124
70
PHR003 Pharyngitis 59 0.122
71
P GLM045 Glioma 61 0.120
72
MSL001 Measles 64 0.119
73
IMM136 Immune System Disease 57 0.119
74
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.118
75
P AMY004 Amyloidosis 69 0.118
76
ALL026 Allergic Hypersensitivity Disease 59 0.116
77
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.113
78
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.112
79
SCK005 Sickle Cell Disease 54 0.112
80
MCR004 Macroglobulinemia 54 0.111
81
MCS002 Mucositis 61 0.110
82
HMN044 Human Immunodeficiency Virus Type 1 71 0.110
83
IMM158 Immune Suppression 57 0.110
84
P CRV035 Cervical Cancer 72 0.108
85
P MMB011 Membranous Nephropathy 55 0.108
86
P PSR002 Psoriasis 65 0.105
87
LYM040 Lymphoblastic Lymphoma 58 0.104
88
P ACT074 Acute Lymphocytic Leukemia 61 0.104
89
RHM027 Rheumatic Disease 62 0.104
90
P PRM006 Primary Biliary Cirrhosis 55 0.104
91
P MDL005 Medulloblastoma 76 0.103
92
P INF032 Infertility 59 0.103
93
SPS003 Spastic Diplegia 55 0.102
94
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.102
95
P PRD008 Periodontitis 67 0.102
96
c LKM063 Leukemia, Chronic Myeloid 80 0.101
97
P BLD134 Bladder Cancer 78 0.101
98
MYL031 Myeloproliferative Neoplasm 64 0.101
99
P HRP006 Herpes Simplex 70 0.100
100
P HMR003 Hemorrhagic Disease 61 0.099
101
P ESP024 Esophagitis 64 0.098
102
DFF005 Diffuse Large B-Cell Lymphoma 64 0.097
103
P UVT001 Uveitis 61 0.097
104
P BLD051 Blood Coagulation Disease 38 0.096
105
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.096
106
LYM067 Lymphoid Leukemia 43 0.096
107
GRW007 Growth Hormone Deficiency 52 0.095
108
PLS009 Plasma Cell Neoplasm 51 0.095
109
VSC008 Vascular Hemostatic Disease 36 0.091
110
LVR012 Liver Cirrhosis 73 0.090
111
ADN018 Adenoma 63 0.090
112
STM007 Stomatitis 52 0.089
113
VTM002 Vitamin B12 Deficiency 46 0.089
114
P EPL164 Epilepsy 70 0.088
115
PST011 Pustulosis of Palm and Sole 47 0.088
116
c WLM018 Wilms Tumor 5 49 0.088
117
URM002 Uremia 52 0.088
118
c BSL007 Basal Cell Carcinoma 66 0.087
119
HYP056 Hypoglycemia 62 0.085
120
P NPH012 Nephrotic Syndrome 60 0.084
121
ENT004 Enthesopathy 38 0.082
122
PLS011 Plasmacytoma 60 0.081
123
P HST010 Histiocytosis 60 0.081
124
c LKM062 Leukemia, Acute Lymphoblastic 64 0.081
125
DWR001 Dwarfism 48 0.080
126
HYP066 Hyperglycemia 64 0.079
127
P RHB003 Rhabdomyosarcoma 61 0.078
128
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 53 0.078
129
P EXN002 Exanthem 62 0.077
130
P CLC063 Celiac Disease 1 65 0.076
131
ORL011 Oral Cancer 60 0.075
132
c SCL052 Scleroderma, Familial Progressive 60 0.075
133
LKP003 Leukoplakia 42 0.075
134
P LRY019 Laryngitis 57 0.074
135
BNF002 Bone Fracture 56 0.073
136
P MNC007 Monocytic Leukemia 59 0.073
137
SMN007 Seminoma 49 0.070
138
MCR013 Microphthalmia 61 0.070
139
P CTR002 Cataract 60 0.069
140
ORL015 Oral Squamous Cell Carcinoma 59 0.069
141
BRN024 Bronchitis 67 0.069
142
CRV038 Cervical Squamous Cell Carcinoma 61 0.068
143
DWN001 Down Syndrome 70 0.065
144
P ICH004 Ichthyosis 54 0.063
145
c SVR001 Severe Acute Respiratory Syndrome 58 0.063
146
P TRC086 Trichohepatoenteric Syndrome 1 54 0.063
147
c INF145 Infantile Liver Failure Syndrome 1 33 0.063
148
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.061
149
MCR093 Microtia-Anotia 24 0.061
150
BRS090 Breast Reconstruction 41 0.059
151
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.057
152
P MCR010 Microcephaly 57 0.057
153
ATS010 Autosomal Recessive Disease 40 0.056
154
c CLR017 Clear Cell Sarcoma 50 0.056
155
P MCK013 Meckel Syndrome, Type 1 62 0.053
156
GRW036 Growth Control, Y-Chromosome Influenced 33 0.052
157
ADL030 Adult-Onset Still's Disease 65 0.052
158
RNL024 Renal Glucosuria 50 0.051
159
c LKM070 Leukemia, Acute Monocytic 55 0.047
160
P TBR001 Tuberous Sclerosis 69 0.047
161
URT010 Ureteral Obstruction 49 0.045
162
FCL068 Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome 27 0.045
163
SKN022 Skin Squamous Cell Carcinoma 46 0.041
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