Search results for isolated anorectal malformation

251 hits were found for isolated anorectal malformation

# Family MCID Name MIFTS Score
1
ISL029 Isolated Anorectal Malformation 7 2.337
2
CRB009 Cerebritis 39 0.178
3
MLN008 Melanoma 62 0.154
4
IMP002 Imperforate Anus 52 0.145
5
P HPT021 Hepatitis 69 0.133
6
FCL044 Fecal Incontinence 35 0.125
7
GRW007 Growth Hormone Deficiency 50 0.124
8
P ADN016 Adenocarcinoma 69 0.123
9
BRT030 Birth Defects 43 0.120
10
ACR041 Acromelic Frontonasal Dysostosis 45 0.120
11
URT001 Urethritis 41 0.113
12
CNS004 Constipation 57 0.108
13
VGN023 Vaginitis 42 0.107
14
RCT017 Rectal Disease 40 0.104
15
THR024 Thrombosis 57 0.103
16
P LKM002 Leukemia 71 0.101
17
NRN002 Neuronitis 41 0.099
18
P ESP024 Esophagitis 61 0.096
19
ANS012 Anus Disease 32 0.093
20
VND001 Vein Disease 47 0.093
21
SRC014 Sarcoma 66 0.090
22
P LYM118 Lymphoma 69 0.089
23
SPL040 Split Hand 36 0.088
24
P TRT010 Teratoma 52 0.088
25
P INT068 Intestinal Disease 60 0.088
26
P HRT032 Heart Disease 75 0.085
27
GST050 Gastrointestinal System Disease 56 0.081
28
P HYP040 Hypospadias 57 0.081
29
P CNG015 Congenital Diaphragmatic Hernia 60 0.081
30
ADN018 Adenoma 58 0.079
31
P HMR003 Hemorrhagic Disease 57 0.079
32
ESP020 Esophageal Atresia 50 0.079
33
ALR002 Al-Raqad Syndrome 36 0.079
34
DDN006 Duodenitis 42 0.078
35
PRS047 Prostatitis 56 0.076
36
P SPL037 Split Hand Foot Malformation 33 0.076
37
P PLM037 Pulmonary Hypertension 79 0.076
38
P END033 Endocarditis 54 0.076
39
CLN019 Colonic Disease 51 0.075
40
MYL020 Myelomeningocele 51 0.075
41
CYS001 Cystic Fibrosis 83 0.074
42
P ART022 Arthritis 75 0.074
43
P HMR012 Hemorrhagic Fever 56 0.073
44
P NRP001 Neuropathy 59 0.072
45
RCT011 Rectal Prolapse 43 0.070
46
SQM006 Squamous Cell Carcinoma 70 0.069
47
MCN001 Mucinous Adenocarcinoma 50 0.069
48
P MCR010 Microcephaly 58 0.069
49
PRD011 Proud Syndrome 42 0.068
50
SPN369 Spinal Disease 39 0.068
51
NRL016 Neural Tube Defects 76 0.068
52
CHR008 Choroiditis 44 0.068
53
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.067
54
PRT036 Peritonitis 63 0.066
55
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.066
56
P PLY006 Polydactyly 56 0.066
57
P RHM011 Rheumatoid Arthritis 89 0.065
58
MCS002 Mucositis 55 0.063
59
SCR024 Sacrococcygeal Teratoma 27 0.063
60
CHL123 Chlamydia 60 0.063
61
ORC001 Orchitis 31 0.062
62
P LVR013 Liver Disease 75 0.062
63
CLN022 Colonic Atresia 24 0.061
64
P NRV007 Nervous System Disease 71 0.061
65
MGC001 Megacolon 45 0.060
66
CLT003 Colitis 60 0.060
67
VSC007 Vascular Disease 67 0.060
68
P CLR023 Colorectal Cancer 97 0.060
69
NRF007 Neurofibroma 53 0.060
70
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.058
71
PLM033 Pulmonary Embolism 60 0.058
72
EPD016 Epidermolysis Bullosa 57 0.058
73
MLR004 Malaria 83 0.058
74
FNC005 Functional Colonic Disease 27 0.058
75
P HRS035 Hirschsprung Disease 1 58 0.057
76
PLM001 Pulmonary Tuberculosis 67 0.057
77
ADL002 Adult Syndrome 52 0.057
78
P BLD051 Blood Coagulation Disease 42 0.057
79
P LPR003 Leprosy 69 0.055
80
CTY001 Cat Eye Syndrome 43 0.055
81
P PYL005 Pyelonephritis 52 0.055
82
P RBL001 Rubella 57 0.055
83
c THR092 Thrombophilia Due to Thrombin Defect 54 0.055
84
P DNR001 Duane Retraction Syndrome 41 0.055
85
P ENC008 Encephalocele 48 0.054
86
c HPT007 Hepatitis E 54 0.053
87
P KDN018 Kidney Disease 66 0.053
88
ACQ007 Acquired Immunodeficiency Syndrome 60 0.053
89
P HMP007 Hemophilia 57 0.053
90
c HYP595 Hypertension, Essential 69 0.053
91
c CNG031 Congenital Nervous System Abnormality 37 0.052
92
P SPN237 Spina Bifida Aperta 34 0.052
93
INF034 Infective Endocarditis 51 0.052
94
SPT005 Spotted Fever 53 0.051
95
ANN002 Anencephaly 54 0.051
96
P INF037 Inflammatory Bowel Disease 63 0.051
97
GST019 Gastrointestinal Stromal Tumor 73 0.051
98
P DYS007 Dyskeratosis Congenita 63 0.051
99
HMR004 Hemorrhagic Fever with Renal Syndrome 58 0.051
100
DWN001 Down Syndrome 66 0.051
101
INT075 Intracranial Hypertension 50 0.051
102
c HPT016 Hepatitis B 64 0.051
103
c HPT003 Hepatitis a 59 0.051
104
P KLP003 Klippel-Feil Syndrome 46 0.050
105
P OBS005 Obesity 92 0.050
106
TTH004 Tethered Spinal Cord Syndrome 31 0.050
107
PLM031 Poliomyelitis 60 0.050
108
DYS073 Dysphagia 48 0.050
109
FCT003 Factor X Deficiency 61 0.050
110
P MMP001 Mumps 58 0.049
111
c SYS001 Systemic Lupus Erythematosus 86 0.049
112
STR067 Stroke, Ischemic 75 0.049
113
c CRN214 Coronary Heart Disease 5 22 0.049
114
P UVT001 Uveitis 58 0.048
115
c HMP029 Hemophilia a 63 0.048
116
DNG002 Dengue Hemorrhagic Fever 63 0.048
117
PLX002 Plexiform Neurofibroma 41 0.048
118
PRP027 Peripheral Vascular Disease 68 0.047
119
P SYP003 Syphilis 53 0.047
120
LNG099 Lung Disease 64 0.047
121
ECH003 Echinococcosis 54 0.046
122
SXL003 Sexual Disorder 42 0.046
123
SPN041 Spinal Cord Disease 51 0.046
124
P MNN007 Meningocele 36 0.045
125
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.045
126
c HMP004 Hemophilia B 62 0.044
127
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.044
128
VNW001 Von Willebrand's Disease 61 0.044
129
c INH004 Inherited Blood Coagulation Disease 36 0.044
130
THR016 Thrombophlebitis 53 0.044
131
PRP030 Purpura 58 0.044
132
P ANT006 Antiphospholipid Syndrome 56 0.044
133
P CHL066 Cholangitis 42 0.044
134
P THR015 Thrombophilia 59 0.043
135
SKN023 Skin Tag 44 0.043
136
SGT001 Sagittal Sinus Thrombosis 35 0.043
137
NRG002 Neurogenic Bladder 50 0.043
138
c ACQ014 Acquired Hemophilia 42 0.043
139
PRS039 Prostate Adenocarcinoma 46 0.043
140
LRN003 Learning Disability 49 0.043
141
P PRN026 Porencephaly 48 0.043
142
VTR016 Vater/vacterl Association 46 0.043
143
P AGG001 Aggressive Periodontitis 50 0.043
144
P HYP620 Hypoprothrombinemia 54 0.042
145
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 0.042
146
P AFB001 Afibrinogenemia 48 0.042
147
PRC002 Paracoccidioidomycosis 55 0.042
148
FCT007 Factor Vii Deficiency 61 0.042
149
PLM010 Pulmonary Edema 54 0.042
150
PRT014 Protein S Deficiency 53 0.042
151
LPT001 Leptospirosis 62 0.041
152
ACT049 Acute Disseminated Encephalomyelitis 49 0.041
153
P PLN008 Peeling Skin Syndrome 45 0.041
154
P PFF001 Pfeiffer Syndrome 73 0.041
155
c BRN108 Branchiootic Syndrome 1 34 0.041
156
ULC004 Ulcerative Colitis 76 0.041
157
P MYS003 Myasthenia Gravis 67 0.041
158
EXF001 Exfoliation Syndrome 57 0.041
159
P CMP008 Compartment Syndrome 48 0.041
160
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.040
161
INT067 Interstitial Nephritis 46 0.040
162
CNN005 Connective Tissue Disease 62 0.040
163
CRD001 Cardiac Tamponade 44 0.040
164
P RTN014 Retinal Artery Occlusion 44 0.040
165
SPC003 Specific Developmental Disorder 38 0.040
166
OCC011 Occipital Encephalocele 24 0.040
167
TRC008 Trachoma 47 0.039
168
RSP006 Respiratory System Disease 58 0.039
169
SPN185 Spinal Cord Infarction 34 0.039
170
SCH014 Schistosomiasis 58 0.039
171
HNT002 Hantavirus Pulmonary Syndrome 51 0.039
172
WHP001 Whipple Disease 49 0.039
173
DDN011 Duodenal Atresia 37 0.039
174
P SPN046 Spinal Muscular Atrophy 65 0.039
175
P STR020 Strabismus 51 0.039
176
P MSC003 Muscular Atrophy 50 0.039
177
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.038
178
APR001 Apraxia 51 0.038
179
HPR003 Heparin-Induced Thrombocytopenia 45 0.038
180
CRB132 Cerebral Sinovenous Thrombosis 31 0.038
181
CRB037 Cerebral Palsy 66 0.038
182
KWS002 Kawasaki Disease 70 0.037
183
MXD005 Mixed Connective Tissue Disease 62 0.037
184
ART017 Aortic Disease 57 0.037
185
PRT011 Protein C Deficiency 52 0.037
186
RPR002 Reproductive System Disease 41 0.037
187
NPH004 Nephropathia Epidemica 40 0.037
188
c ATM011 Autoimmune Hepatitis 60 0.037
189
PLS007 Plasmodium Falciparum Malaria 55 0.037
190
CHN016 Cohen Syndrome 54 0.037
191
HYP037 Hyperhomocysteinemia 50 0.037
192
CRV043 Cervical Dystonia 44 0.037
193
RCR004 Recurrent Respiratory Papillomatosis 42 0.037
194
SPN186 Spinal Cord Injury 63 0.035
195
FCT006 Factor V Deficiency 57 0.035
196
DSS009 Disseminated Intravascular Coagulation 51 0.035
197
PNL023 Penile Agenesis 21 0.035
198
P NRC002 Narcolepsy 62 0.035
199
P ADL010 Adult Respiratory Distress Syndrome 61 0.035
200
FCT004 Factor Xii Deficiency 50 0.035
201
PST095 Post-Thrombotic Syndrome 47 0.035
202
ADT003 Auditory System Disease 40 0.035
203
LVD002 Livedoid Vasculopathy 32 0.035
204
FLR002 Filariasis 54 0.035
205
INT051 Intussusception 50 0.035
206
END021 Endomyocardial Fibrosis 49 0.035
207
c CLR085 Colorectal Cancer 1 45 0.035
208
SXD001 Sex Differentiation Disease 38 0.035
209
LMY002 Leiomyoma 54 0.034
210
IMM136 Immune System Disease 51 0.034
211
HMR002 Hemarthrosis 48 0.034
212
LYM008 Lymphangiosarcoma 47 0.034
213
LPB001 Lipoblastoma 34 0.034
214
WST001 West Syndrome 57 0.033
215
VRL011 Viral Infectious Disease 55 0.033
216
BLD053 Blood Platelet Disease 46 0.033
217
DSC009 Discoid Lupus Erythematosus 45 0.033
218
LCH009 Lichen Sclerosus 41 0.033
219
SPC005 Speech Disorder 41 0.033
220
P HYP263 Hypersomnia 40 0.033
221
P ATM020 Autoimmune Enteropathy 39 0.033
222
EPD018 Epididymo-Orchitis 30 0.033
223
WGN006 Wegener Granulomatosis 63 0.032
224
GLL022 Guillain-Barre Syndrome 56 0.032
225
P BDD001 Budd-Chiari Syndrome 56 0.032
226
RHM028 Rheumatic Heart Disease 50 0.032
227
P PNV001 Panuveitis 50 0.032
228
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 0.032
229
PLC007 Placental Abruption 47 0.032
230
c INT072 Intestinal Pseudo-Obstruction 46 0.032
231
IDP024 Idiopathic Inflammatory Myopathy 46 0.032
232
PNT038 Peanut Allergy 44 0.032
233
c HMG003 Hemoglobin E Disease 44 0.032
234
P PRP034 Purpura Fulminans 41 0.032
235
ENT001 Enterocele 40 0.032
236
LCH001 Leech Infestation 40 0.032
237
FCL010 Focal Epithelial Hyperplasia 38 0.032
238
AMY002 Amyloid Tumor 37 0.032
239
PRC051 Paracetamol Poisoning 27 0.032
240
c VRL010 Viral Hepatitis 60 0.030
241
MCR088 Microscopic Polyangiitis 49 0.030
242
c ATM024 Autoimmune Pancreatitis 47 0.030
243
FCT005 Factor Xiii Deficiency 43 0.030
244
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.030
245
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 0.030
246
P CYS017 Cystic Teratoma 40 0.030
247
MLR007 Male Reproductive System Disease 34 0.030
248
SWL001 Swallowing Disorders 33 0.030
249
QLT001 Qualitative Platelet Defect 32 0.030
250
CYT014 Cytochrome P450 Oxidoreductase Deficiency 27 0.030
251
c CRN177 Coronary Heart Disease 7 20 0.030
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