Search results for isolated anorectal malformation

127 hits were found for isolated anorectal malformation

# Family MCID Name MIFTS Score
1
ISL029 Isolated Anorectal Malformation 6 2.338
2
ART005 Arteriovenous Malformation 64 0.251
3
CRB009 Cerebritis 41 0.203
4
MLN008 Melanoma 72 0.186
5
ANR033 Anorectal Anomalies 24 0.183
6
ANS023 Anus, Imperforate 50 0.181
7
FCL044 Fecal Incontinence 38 0.165
8
P ADN016 Adenocarcinoma 71 0.144
9
GST050 Gastrointestinal System Disease 66 0.141
10
URT001 Urethritis 44 0.137
11
VGN023 Vaginitis 59 0.135
12
CNS004 Constipation 57 0.134
13
P ANR048 Aniridia 1 68 0.133
14
P HRT032 Heart Disease 80 0.133
15
GRW007 Growth Hormone Deficiency 52 0.130
16
P PNC044 Pancreatitis 64 0.128
17
ANR038 Anorexia Nervosa 1 21 0.125
18
BLD137 Blood Group--Ahonen 17 0.125
19
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.117
20
AGN016 Aging 65 0.112
21
NRN002 Neuronitis 43 0.112
22
P LKM002 Leukemia 75 0.111
23
P ESP024 Esophagitis 64 0.110
24
P TRT010 Teratoma 53 0.108
25
SPL040 Split Hand 34 0.105
26
P HMN010 Hemangioma 61 0.101
27
SRC014 Sarcoma 68 0.099
28
ESP020 Esophageal Atresia 54 0.099
29
P LYM118 Lymphoma 71 0.098
30
THR024 Thrombosis 61 0.095
31
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 36 0.095
32
CLF027 Cleft Palate, Isolated 61 0.094
33
NRL016 Neural Tube Defects 79 0.094
34
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.093
35
P SPL061 Split Hand-Foot Malformation 41 0.093
36
P HYP040 Hypospadias 60 0.091
37
c DPH024 Diaphragmatic Hernia, Congenital 63 0.090
38
P PLV020 Pelvic Organ Prolapse 63 0.090
39
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.089
40
DDN006 Duodenitis 46 0.089
41
ADN018 Adenoma 63 0.089
42
P HRS035 Hirschsprung Disease 1 64 0.088
43
P PLY006 Polydactyly 57 0.088
44
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.087
45
MCN001 Mucinous Adenocarcinoma 54 0.087
46
SQM006 Squamous Cell Carcinoma 74 0.086
47
P MLT020 Multiple Sclerosis 85 0.085
48
P RNL100 Renal Hypodysplasia/aplasia 1 57 0.084
49
P PLM037 Pulmonary Hypertension 79 0.083
50
HPT082 Hepatic Adenomas, Familial 52 0.082
51
CYS001 Cystic Fibrosis 85 0.081
52
P ART022 Arthritis 77 0.081
53
MYL020 Myelomeningocele 54 0.081
54
P NRP001 Neuropathy 63 0.079
55
P MCR010 Microcephaly 57 0.079
56
P NRV007 Nervous System Disease 75 0.078
57
CLB010 Coloboma of Macula 52 0.078
58
SCR024 Sacrococcygeal Teratoma 32 0.078
59
MGC001 Megacolon 50 0.077
60
CTY001 Cat Eye Syndrome 49 0.075
61
ORC001 Orchitis 34 0.074
62
MCS002 Mucositis 61 0.074
63
c BRN108 Branchiootic Syndrome 1 47 0.072
64
PFF001 Pfeiffer Syndrome 74 0.071
65
PHR003 Pharyngitis 59 0.071
66
EPD016 Epidermolysis Bullosa 57 0.070
67
VSC007 Vascular Disease 71 0.069
68
CLT003 Colitis 63 0.069
69
LNG099 Lung Disease 67 0.069
70
P ENC008 Encephalocele 48 0.067
71
P KDN018 Kidney Disease 69 0.065
72
VTR016 Vater/vacterl Association 37 0.064
73
BFD001 Bifid Nose 22 0.064
74
GST019 Gastrointestinal Stromal Tumor 74 0.063
75
DWN001 Down Syndrome 70 0.063
76
P KLP003 Klippel-Feil Syndrome 46 0.061
77
P DYS007 Dyskeratosis Congenita 68 0.060
78
P DNR001 Duane Retraction Syndrome 44 0.060
79
DYS073 Dysphagia 47 0.060
80
P PYL005 Pyelonephritis 56 0.059
81
P KBK002 Kabuki Syndrome 1 62 0.058
82
PSD009 Pseudohermaphroditism 42 0.058
83
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.057
84
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.057
85
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.057
86
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.057
87
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.057
88
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.057
89
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.057
90
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.057
91
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.057
92
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.056
93
c FRS014 Fraser Syndrome 1 51 0.056
94
NRG002 Neurogenic Bladder 53 0.056
95
RNL078 Renal Dysplasia 49 0.054
96
P MNN007 Meningocele 38 0.054
97
VCT001 Vacterl Association 41 0.053
98
ANG011 Angiodysplasia 48 0.052
99
PYL012 Pyloric Atresia 34 0.052
100
PPL022 Papilloma 58 0.051
101
RSP006 Respiratory System Disease 63 0.051
102
c ACT027 Acute Pancreatitis 61 0.051
103
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.049
104
P TRC086 Trichohepatoenteric Syndrome 1 54 0.049
105
DDN011 Duodenal Atresia 39 0.049
106
OCC011 Occipital Encephalocele 25 0.049
107
CLN022 Colonic Atresia 27 0.049
108
HYP748 Hypertelorism 46 0.048
109
INT067 Interstitial Nephritis 51 0.047
110
VLC001 Velocardiofacial Syndrome 64 0.047
111
c PST041 Posterior Urethral Valves 51 0.047
112
ULC004 Ulcerative Colitis 80 0.045
113
THR016 Thrombophlebitis 53 0.045
114
c ATR062 Atrial Septal Defect 1 32 0.043
115
LPB001 Lipoblastoma 38 0.043
116
PNL023 Penile Agenesis 25 0.042
117
c BRT038 Baraitser-Winter Syndrome 1 37 0.041
118
PLY150 Polykaryocytosis Inducer 20 0.041
119
INT051 Intussusception 51 0.041
120
CHN016 Cohen Syndrome 48 0.041
121
SPN186 Spinal Cord Injury 67 0.040
122
LMY002 Leiomyoma 58 0.040
123
c INT072 Intestinal Pseudo-Obstruction 57 0.040
124
P UTR058 Uterine Anomalies 55 0.039
125
EPD018 Epididymo-Orchitis 33 0.039
126
GNT050 Genitourinary Tract Anomalies 41 0.039
127
P CYS017 Cystic Teratoma 40 0.039
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