Search results for isolated anorectal malformation

143 hits were found for isolated anorectal malformation

# Family MCID Name MIFTS Score
1
ISL029 Isolated Anorectal Malformation 7 2.346
2
ART005 Arteriovenous Malformation 63 0.232
3
CRB009 Cerebritis 39 0.193
4
MLN008 Melanoma 70 0.174
5
IMP002 Imperforate Anus 52 0.163
6
BRT030 Birth Defects 44 0.144
7
FCL044 Fecal Incontinence 34 0.140
8
P ADN016 Adenocarcinoma 69 0.136
9
GRW007 Growth Hormone Deficiency 48 0.131
10
P PNC044 Pancreatitis 60 0.126
11
URT001 Urethritis 40 0.125
12
VSC047 Vascular Malformation 43 0.123
13
VGN023 Vaginitis 41 0.122
14
CNS004 Constipation 56 0.120
15
GST050 Gastrointestinal System Disease 53 0.117
16
P LKM002 Leukemia 72 0.107
17
NRN002 Neuronitis 39 0.107
18
P HRT032 Heart Disease 75 0.106
19
P ESP024 Esophagitis 59 0.104
20
SRC014 Sarcoma 66 0.097
21
SPL040 Split Hand 36 0.097
22
P TRT010 Teratoma 51 0.096
23
P LYM118 Lymphoma 69 0.094
24
P HMN010 Hemangioma 59 0.094
25
THR024 Thrombosis 43 0.093
26
ESP020 Esophageal Atresia 50 0.091
27
VND001 Vein Disease 49 0.090
28
ANS012 Anus Disease 31 0.089
29
P HYP040 Hypospadias 58 0.087
30
P CNG015 Congenital Diaphragmatic Hernia 60 0.087
31
P SPL061 Split Hand-Foot Malformation 35 0.085
32
DDN006 Duodenitis 40 0.085
33
ADN018 Adenoma 58 0.084
34
P CLR023 Colorectal Cancer 95 0.083
35
P PLM037 Pulmonary Hypertension 77 0.082
36
PRS047 Prostatitis 55 0.082
37
SQM006 Squamous Cell Carcinoma 69 0.081
38
CYS001 Cystic Fibrosis 86 0.079
39
ADL002 Adult Syndrome 57 0.079
40
RCT011 Rectal Prolapse 41 0.079
41
P NRP001 Neuropathy 57 0.077
42
MCN001 Mucinous Adenocarcinoma 49 0.077
43
P ART022 Arthritis 72 0.076
44
P MCR010 Microcephaly 58 0.075
45
MYL020 Myelomeningocele 50 0.075
46
CLB001 Coloboma 54 0.072
47
P HMR003 Hemorrhagic Disease 55 0.072
48
P NRV007 Nervous System Disease 70 0.072
49
P PLY006 Polydactyly 54 0.071
50
SCR024 Sacrococcygeal Teratoma 27 0.070
51
MCS002 Mucositis 54 0.070
52
VSC007 Vascular Disease 65 0.068
53
ORC001 Orchitis 32 0.068
54
CLN022 Colonic Atresia 25 0.067
55
MGC001 Megacolon 46 0.067
56
FNC005 Functional Colonic Disease 30 0.067
57
EPD016 Epidermolysis Bullosa 55 0.067
58
CLT003 Colitis 58 0.066
59
ART111 Artery Disease 55 0.066
60
P OBS005 Obesity 91 0.065
61
P GST049 Gastrointestinal System Cancer 59 0.064
62
DWN001 Down Syndrome 69 0.061
63
P KDN018 Kidney Disease 65 0.061
64
P ANR002 Aniridia 66 0.061
65
CTY001 Cat Eye Syndrome 43 0.060
66
P INT063 Intellectual Disability 58 0.060
67
GST019 Gastrointestinal Stromal Tumor 74 0.059
68
P DNR001 Duane Retraction Syndrome 43 0.059
69
NRL016 Neural Tube Defects 76 0.059
70
P ENC008 Encephalocele 48 0.058
71
P PYL005 Pyelonephritis 52 0.058
72
BFD001 Bifid Nose 26 0.058
73
P HRS035 Hirschsprung Disease 1 58 0.057
74
c CNG031 Congenital Nervous System Abnormality 39 0.056
75
SNS001 Sensorineural Hearing Loss 54 0.056
76
P DYS007 Dyskeratosis Congenita 66 0.055
77
P KLP003 Klippel-Feil Syndrome 44 0.055
78
DYS073 Dysphagia 47 0.055
79
LNG099 Lung Disease 61 0.053
80
SPN369 Spinal Disease 38 0.052
81
P CTR002 Cataract 57 0.052
82
NRG002 Neurogenic Bladder 50 0.051
83
RPR002 Reproductive System Disease 43 0.051
84
PHY002 Physical Disorder 43 0.051
85
PTR032 Peters-Plus Syndrome 59 0.050
86
SKN023 Skin Tag 46 0.050
87
P BLD051 Blood Coagulation Disease 43 0.050
88
P FRS014 Fraser Syndrome 1 51 0.050
89
P TRC086 Trichohepatoenteric Syndrome 1 51 0.049
90
RNL078 Renal Dysplasia 50 0.049
91
P MNN007 Meningocele 35 0.049
92
VSC006 Vascular Cancer 52 0.048
93
PPL022 Papilloma 54 0.048
94
ACQ007 Acquired Immunodeficiency Syndrome 60 0.048
95
RSP006 Respiratory System Disease 60 0.048
96
c ACT027 Acute Pancreatitis 56 0.048
97
ANG011 Angiodysplasia 43 0.048
98
c PND001 Pain Disorder 55 0.047
99
c BRN108 Branchiootic Syndrome 1 35 0.047
100
P PFF001 Pfeiffer Syndrome 71 0.046
101
VCT001 Vacterl Association 40 0.046
102
RDT013 Radiation Proctitis 46 0.046
103
DDN011 Duodenal Atresia 37 0.046
104
P ART023 Arthropathy 62 0.045
105
FCT007 Factor Vii Deficiency 59 0.045
106
ULC004 Ulcerative Colitis 72 0.045
107
P PLN008 Peeling Skin Syndrome 49 0.045
108
VTR016 Vater/vacterl Association 39 0.045
109
VRL011 Viral Infectious Disease 59 0.044
110
P AXN002 Axenfeld-Rieger Syndrome 51 0.044
111
INT067 Interstitial Nephritis 45 0.044
112
OCC011 Occipital Encephalocele 23 0.043
113
P HMP007 Hemophilia 55 0.042
114
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 41 0.042
115
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 41 0.042
116
P MNC007 Monocytic Leukemia 54 0.041
117
c CTR130 Cataract 9, Multiple Types 40 0.041
118
CNG005 Congenital Aphakia 33 0.041
119
CRD001 Cardiac Tamponade 43 0.040
120
c PST041 Posterior Urethral Valves 46 0.040
121
SPN186 Spinal Cord Injury 62 0.039
122
LMY002 Leiomyoma 53 0.039
123
P ANT073 Anterior Segment Dysgenesis 1, Multiple Subtypes 40 0.039
124
PNL023 Penile Agenesis 23 0.039
125
CHN016 Cohen Syndrome 54 0.038
126
P USH001 Usher Syndrome 54 0.038
127
ESP023 Esophageal Disease 50 0.038
128
HMR002 Hemarthrosis 47 0.037
129
LPB001 Lipoblastoma 34 0.037
130
c ANT068 Anterior Segment Dysgenesis 2, Multiple Subtypes 31 0.037
131
P UTR038 Uterine Disease 36 0.036
132
EPD018 Epididymo-Orchitis 30 0.036
133
MRN009 Morning Glory Syndrome 26 0.036
134
P THR015 Thrombophilia 58 0.035
135
c INT072 Intestinal Pseudo-Obstruction 41 0.035
136
c HMP004 Hemophilia B 62 0.033
137
WST001 West Syndrome 58 0.033
138
PRP036 Peripheral T-Cell Lymphoma 42 0.033
139
ADT003 Auditory System Disease 41 0.033
140
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 39 0.033
141
P CYS017 Cystic Teratoma 38 0.033
142
MLR007 Male Reproductive System Disease 36 0.033
143
P SCL047 Sclerocornea 27 0.033
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