Search results for fanconi anemia, complementation group m

202 hits were found for fanconi anemia, complementation group m

# Family MCID Name MIFTS Score
1
P LKM002 Leukemia 71 0.425
2
P HPT021 Hepatitis 69 0.295
3
c FNC027 Fanconi Anemia, Complementation Group a 71 0.288
4
P BRS047 Breast Cancer 100 0.270
5
P LYM118 Lymphoma 69 0.265
6
P MYL006 Myeloid Leukemia 66 0.211
7
MYL009 Myelodysplastic Syndrome 73 0.209
8
SQM006 Squamous Cell Carcinoma 70 0.200
9
MRG013 Mirage Syndrome 29 0.197
10
P LNG032 Lung Cancer 95 0.188
11
P KDN018 Kidney Disease 66 0.180
12
NTR005 Nutritional Deficiency Disease 36 0.176
13
HMT018 Hematopoietic Stem Cell Transplantation 41 0.174
14
P MLT019 Multiple Myeloma 83 0.169
15
RFR010 Refractory Anemia 45 0.168
16
P PNM007 Pneumonia 68 0.166
17
BNM001 Bone Marrow Cancer 51 0.166
18
c ACT073 Acute Leukemia 60 0.163
19
P ADN016 Adenocarcinoma 69 0.162
20
MLN008 Melanoma 62 0.160
21
P KDN017 Kidney Cancer 65 0.158
22
RTN023 Retinitis 50 0.157
23
SRC014 Sarcoma 66 0.157
24
c CHR090 Chronic Lymphocytic Leukemia 76 0.155
25
P GLM007 Glomerulonephritis 59 0.155
26
HMT002 Hematologic Cancer 64 0.153
27
P LYM026 Lymphoblastic Leukemia 62 0.152
28
BNC003 Bone Cancer 58 0.150
29
CHL071 Child Syndrome 58 0.150
30
KDS001 Kid Syndrome 53 0.150
31
P HPT023 Hepatocellular Carcinoma 92 0.150
32
PRM243 Primary Bone Cancer 29 0.149
33
c CHR089 Chronic Kidney Failure 66 0.148
34
P PNC044 Pancreatitis 61 0.146
35
c INH020 Inherited Metabolic Disorder 49 0.146
36
P ATX004 Ataxia 53 0.143
37
P HRT032 Heart Disease 75 0.143
38
BNS002 Bone Structure Disease 37 0.142
39
P THY032 Thyroiditis 54 0.140
40
P OVR042 Ovarian Cancer 76 0.139
41
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.139
42
c HPT016 Hepatitis B 64 0.135
43
THR024 Thrombosis 57 0.135
44
P CLR023 Colorectal Cancer 97 0.134
45
BLD054 Blood Protein Disease 37 0.134
46
HV1006 Hiv-1 80 0.133
47
PCK002 Pick Disease 68 0.133
48
CSY001 C Syndrome 50 0.129
49
IMP003 Impaired Renal Function Disease 34 0.129
50
ADJ001 Adjustment Disorder 38 0.127
51
ISC004 Ischemia 61 0.127
52
BLD053 Blood Platelet Disease 46 0.126
53
P BCL006 B-Cell Lymphomas 65 0.126
54
P INF038 Influenza 72 0.125
55
END030 End Stage Renal Failure 55 0.123
56
P MYP004 Myopathy 67 0.123
57
P NRB001 Neuroblastoma 70 0.123
58
c CHR418 Chronic Leukemia 47 0.122
59
P ATX030 Ataxia-Telangiectasia 77 0.121
60
ALR002 Al-Raqad Syndrome 36 0.121
61
PHR003 Pharyngitis 56 0.116
62
P AST005 Asthma 82 0.115
63
P CRV039 Cervicitis 45 0.115
64
c LKM061 Leukemia, Acute Myeloid 73 0.113
65
P PNC035 Pancreatic Cancer 87 0.113
66
P RNL014 Renal Cell Carcinoma 82 0.112
67
INC022 Inclusion-Cell Disease 46 0.111
68
ACT118 Acute Non Lymphoblastic Leukemia 30 0.110
69
P TCL004 T-Cell Leukemia 47 0.109
70
c CHR064 Chronic Monocytic Leukemia 42 0.106
71
GDS001 Good Syndrome 44 0.105
72
P GLM045 Glioma 60 0.105
73
LKC003 Leukocyte Disease 43 0.104
74
MSL001 Measles 61 0.104
75
WLL006 Wells Syndrome 59 0.104
76
HYP266 Hypoxia 56 0.103
77
c RNL016 Renal Infectious Disease 20 0.103
78
SXL003 Sexual Disorder 42 0.103
79
PRP021 Peripheral Nervous System Neoplasm 46 0.102
80
P MDL005 Medulloblastoma 77 0.101
81
c ADL017 Adult T-Cell Leukemia 60 0.101
82
MCS002 Mucositis 55 0.100
83
PRM025 Primary Bacterial Infectious Disease 41 0.100
84
P AMY004 Amyloidosis 65 0.100
85
P PRM006 Primary Biliary Cirrhosis 51 0.097
86
P PSR002 Psoriasis 61 0.097
87
ACQ007 Acquired Immunodeficiency Syndrome 60 0.097
88
P ACT074 Acute Lymphocytic Leukemia 56 0.097
89
ACR041 Acromelic Frontonasal Dysostosis 45 0.095
90
BRT030 Birth Defects 43 0.095
91
PRP027 Peripheral Vascular Disease 68 0.095
92
SKN016 Skin Disease 66 0.095
93
P PRD008 Periodontitis 63 0.095
94
P MMB011 Membranous Nephropathy 54 0.094
95
P LYM033 Lymphoproliferative Syndrome 56 0.093
96
P HRP006 Herpes Simplex 65 0.092
97
HRT007 Heart Cancer 46 0.091
98
P HRT017 Heart Tumor 32 0.091
99
c ADL079 Adult Heart Tumor 16 0.091
100
CRD118 Cardiovascular Cancer 44 0.091
101
P ESP024 Esophagitis 61 0.091
102
PRM097 Primary Immunodeficiency Disease 60 0.091
103
P INF032 Infertility 59 0.090
104
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.089
105
DMN002 Dementia 65 0.089
106
DFF005 Diffuse Large B-Cell Lymphoma 59 0.088
107
RHM027 Rheumatic Disease 58 0.088
108
c ACT071 Acute Kidney Failure 49 0.088
109
VSC008 Vascular Hemostatic Disease 30 0.088
110
P BLD051 Blood Coagulation Disease 42 0.087
111
ALN001 Aland Island Eye Disease 45 0.087
112
VSC006 Vascular Cancer 51 0.087
113
P ENC018 Encephalopathy 59 0.087
114
P SKN013 Skin Benign Neoplasm 43 0.087
115
MYL031 Myeloproliferative Neoplasm 58 0.087
116
LYM024 Lymphatic System Disease 52 0.087
117
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.086
118
TCL003 T Cell Deficiency 45 0.086
119
P HMR003 Hemorrhagic Disease 57 0.086
120
c CRN214 Coronary Heart Disease 5 22 0.085
121
PLS009 Plasma Cell Neoplasm 48 0.084
122
ACD009 Acid-Labile Subunit, Deficiency of 45 0.084
123
LYM067 Lymphoid Leukemia 44 0.084
124
ORL011 Oral Cancer 56 0.083
125
P NRV006 Nervous System Cancer 60 0.081
126
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.080
127
P SPS003 Spastic Diplegia 52 0.080
128
LYM023 Lymphatic System Cancer 33 0.079
129
CNN005 Connective Tissue Disease 62 0.079
130
ATN003 Autonomic Nervous System Neoplasm 40 0.079
131
ATN002 Autonomic Nervous System Disease 48 0.078
132
P EPL164 Epilepsy 66 0.078
133
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.078
134
P CLC005 Celiac Disease 68 0.077
135
OCL009 Ocular Cancer 59 0.077
136
SKN023 Skin Tag 44 0.077
137
ALL026 Allergic Hypersensitivity Disease 52 0.077
138
c LKM062 Leukemia, Acute Lymphoblastic 64 0.076
139
P PLN008 Peeling Skin Syndrome 45 0.075
140
DWN001 Down Syndrome 66 0.074
141
LVR012 Liver Cirrhosis 67 0.073
142
EXF001 Exfoliation Syndrome 57 0.073
143
P NPH012 Nephrotic Syndrome 59 0.073
144
STM007 Stomatitis 50 0.073
145
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.072
146
CTS003 Coats Disease 57 0.072
147
ADN018 Adenoma 58 0.071
148
HRT029 Heart Tumor of the Child 15 0.071
149
P EXN002 Exanthem 57 0.071
150
BNL002 Bone Lymphoma 32 0.070
151
CRV038 Cervical Squamous Cell Carcinoma 60 0.069
152
URM002 Uremia 48 0.069
153
P HST010 Histiocytosis 58 0.068
154
ATR060 Atrial Standstill, Digenic 51 0.067
155
c CLL013 Cell Type Cancer 46 0.067
156
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.067
157
c LKM004 Leukemia, B-Cell, Chronic 24 0.067
158
c CRN173 Coronary Heart Disease 8 18 0.066
159
WST001 West Syndrome 57 0.065
160
c PLN018 Peeling Skin Syndrome 2 40 0.064
161
SPC003 Specific Developmental Disorder 38 0.064
162
DWR001 Dwarfism 47 0.063
163
P MNC007 Monocytic Leukemia 55 0.062
164
c BSL007 Basal Cell Carcinoma 65 0.062
165
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.062
166
RNL101 Renal Cell Carcinoma, Papillary 63 0.062
167
c LKM050 Leukemia, Chronic Lymphocytic 1 19 0.061
168
ORL015 Oral Squamous Cell Carcinoma 57 0.061
169
MTR014 Motor Neuron Disease 58 0.060
170
P LTR001 Lateral Sclerosis 53 0.060
171
PRD011 Proud Syndrome 42 0.059
172
c PLN017 Peeling Skin Syndrome 1 34 0.059
173
c LKM051 Leukemia, Chronic Lymphocytic 3 19 0.059
174
SNS023 Sensory System Cancer 43 0.058
175
GLC077 Glucocorticoid Therapy, Response to 16 0.058
176
c DLT002 Dilated Cardiomyopathy 76 0.058
177
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.058
178
MXD023 Mixed Cell Type Cancer 44 0.058
179
CNT018 Central Nervous System Leukemia 37 0.057
180
BNF002 Bone Fracture 50 0.057
181
P GND004 Gonadal Dysgenesis 51 0.057
182
P ICH004 Ichthyosis 52 0.057
183
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.056
184
PRN023 Prion Disease 48 0.055
185
CRN017 Coronary Thrombosis 48 0.055
186
ADR038 Adermatoglyphia 46 0.053
187
P PTS002 Ptosis 51 0.052
188
MCR013 Microphthalmia 60 0.052
189
FCT008 Factitious Disorder 41 0.049
190
ADL030 Adult-Onset Still's Disease 59 0.048
191
P MCR010 Microcephaly 58 0.048
192
P SJG001 Sjogren's Syndrome 50 0.048
193
FBR054 Fibroma 46 0.048
194
c ACT009 Acute Monocytic Leukemia 52 0.047
195
AMB002 Amblyopia 46 0.046
196
SCT005 Scott Syndrome 53 0.044
197
P XLN007 X-Linked Disease 34 0.043
198
IMM025 Immunoglobulin a Deficiency 2 24 0.042
199
P CRB019 Cerebral Amyloid Angiopathy 58 0.042
200
MTG002 Mutagen Sensitivity 36 0.042
201
RGH001 Right Bundle Branch Block 44 0.039
202
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.039
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