Search results for "isolated anorectal malformation"

The MalaCard for "isolated anorectal malformation" has been retired.
Searching MalaCards for entries containing "isolated anorectal malformation"

150 hits were found for 'isolated anorectal malformation'

# Family MCID Name MIFTS Score
1
ISL029 Isolated Anorectal Malformation 7 2.344
2
CRB009 Cerebritis 38 0.186
3
IMP002 Imperforate Anus 52 0.162
4
FCL044 Fecal Incontinence 35 0.142
5
P ADN016 Adenocarcinoma 69 0.134
6
GRW007 Growth Hormone Deficiency 48 0.132
7
URT001 Urethritis 40 0.124
8
CNS004 Constipation 57 0.123
9
ACR041 Acromelic Frontonasal Dysostosis 46 0.119
10
BRT030 Birth Defects 43 0.118
11
VGN023 Vaginitis 42 0.117
12
RCT017 Rectal Disease 39 0.115
13
P LKM002 Leukemia 70 0.109
14
NRN002 Neuronitis 42 0.107
15
P ESP024 Esophagitis 62 0.106
16
P INT068 Intestinal Disease 61 0.105
17
ANS012 Anus Disease 32 0.100
18
P TRT010 Teratoma 52 0.098
19
SRC014 Sarcoma 66 0.097
20
P LYM118 Lymphoma 70 0.096
21
SPL040 Split Hand 37 0.092
22
VND001 Vein Disease 52 0.091
23
P HRT032 Heart Disease 76 0.089
24
GST050 Gastrointestinal System Disease 54 0.087
25
P HYP040 Hypospadias 57 0.086
26
ESP020 Esophageal Atresia 49 0.085
27
ADN018 Adenoma 59 0.085
28
PRS047 Prostatitis 56 0.084
29
DDN006 Duodenitis 44 0.084
30
P CNG015 Congenital Diaphragmatic Hernia 58 0.084
31
P ART022 Arthritis 75 0.082
32
P PLM037 Pulmonary Hypertension 79 0.081
33
ALR002 Al-Raqad Syndrome 36 0.081
34
CYS001 Cystic Fibrosis 86 0.080
35
CLN019 Colonic Disease 50 0.079
36
RCT011 Rectal Prolapse 43 0.079
37
MCN001 Mucinous Adenocarcinoma 50 0.079
38
P NRP001 Neuropathy 60 0.076
39
P SPL037 Split Hand Foot Malformation 32 0.076
40
P HMR003 Hemorrhagic Disease 57 0.075
41
P MCR010 Microcephaly 58 0.072
42
CHL123 Chlamydia 59 0.071
43
SCR024 Sacrococcygeal Teratoma 26 0.070
44
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.070
45
ORC001 Orchitis 34 0.069
46
MGC001 Megacolon 50 0.068
47
CLN022 Colonic Atresia 24 0.068
48
P PLY006 Polydactyly 55 0.067
49
SPN369 Spinal Disease 41 0.066
50
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.065
51
VSC007 Vascular Disease 67 0.064
52
CLT003 Colitis 59 0.064
53
EPD016 Epidermolysis Bullosa 57 0.064
54
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.064
55
ADL002 Adult Syndrome 53 0.063
56
P HRS035 Hirschsprung Disease 1 59 0.062
57
PRD011 Proud Syndrome 42 0.061
58
ANR002 Aniridia 60 0.061
59
P PYL005 Pyelonephritis 52 0.061
60
CTY001 Cat Eye Syndrome 42 0.061
61
FNC005 Functional Colonic Disease 30 0.061
62
P ENC008 Encephalocele 47 0.060
63
P NRV007 Nervous System Disease 71 0.059
64
DMY004 Demyelinating Disease 55 0.058
65
P END047 Endophthalmitis 46 0.057
66
INT060 Intestinal Atresia 40 0.057
67
c HYP595 Hypertension, Essential 69 0.056
68
P KLP003 Klippel-Feil Syndrome 46 0.056
69
SNS001 Sensorineural Hearing Loss 57 0.055
70
P OBS005 Obesity 93 0.055
71
NRL016 Neural Tube Defects 76 0.055
72
GST019 Gastrointestinal Stromal Tumor 72 0.054
73
DYS073 Dysphagia 49 0.054
74
DWN001 Down Syndrome 65 0.053
75
PTR006 Peters Anomaly 64 0.053
76
c CRN214 Coronary Heart Disease 5 23 0.053
77
PRP027 Peripheral Vascular Disease 69 0.052
78
LNG099 Lung Disease 62 0.052
79
P BLD051 Blood Coagulation Disease 45 0.051
80
SKN016 Skin Disease 68 0.051
81
SXL003 Sexual Disorder 47 0.051
82
c CNG031 Congenital Nervous System Abnormality 39 0.051
83
KDS001 Kid Syndrome 53 0.050
84
ADT003 Auditory System Disease 51 0.049
85
SPN041 Spinal Cord Disease 48 0.049
86
P MNN007 Meningocele 36 0.049
87
SKN023 Skin Tag 46 0.048
88
P CTR002 Cataract 57 0.048
89
NRG002 Neurogenic Bladder 50 0.047
90
RSP006 Respiratory System Disease 62 0.047
91
INT253 Intestinal Benign Neoplasm 50 0.047
92
P DYS007 Dyskeratosis Congenita 63 0.047
93
LRN003 Learning Disability 51 0.046
94
RCT018 Rectal Neoplasm 55 0.046
95
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.045
96
FCT007 Factor Vii Deficiency 62 0.045
97
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.045
98
VTR016 Vater/vacterl Association 46 0.045
99
P PLN008 Peeling Skin Syndrome 47 0.045
100
P PFF001 Pfeiffer Syndrome 73 0.045
101
c BRN108 Branchiootic Syndrome 1 36 0.045
102
ESP023 Esophageal Disease 53 0.044
103
INT067 Interstitial Nephritis 47 0.044
104
P MNC007 Monocytic Leukemia 55 0.044
105
CRD001 Cardiac Tamponade 44 0.044
106
P ART023 Arthropathy 63 0.044
107
c PTS008 Ptosis, Congenital 32 0.044
108
SPC003 Specific Developmental Disorder 40 0.044
109
ULC004 Ulcerative Colitis 75 0.043
110
GLB003 Globe Disease 35 0.043
111
P ANT026 Anterior Segment Mesenchymal Dysgenesis 38 0.043
112
OCC011 Occipital Encephalocele 23 0.043
113
P HMP007 Hemophilia 56 0.043
114
TNG009 Tongue Squamous Cell Carcinoma 74 0.042
115
P DNR003 Duane Retraction Syndrome 1 39 0.042
116
DDN011 Duodenal Atresia 39 0.042
117
SYS003 Systolic Heart Failure 43 0.042
118
c PST041 Posterior Urethral Valves 46 0.041
119
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 44 0.041
120
RPR002 Reproductive System Disease 46 0.041
121
CNG069 Congenital Cytomegalovirus 34 0.040
122
P RTH001 Rothmund-Thomson Syndrome 57 0.040
123
SPN186 Spinal Cord Injury 62 0.039
124
c INH004 Inherited Blood Coagulation Disease 39 0.039
125
PNL023 Penile Agenesis 20 0.039
126
c INF067 Inflammatory Bowel Disease 10 51 0.038
127
CHN016 Cohen Syndrome 55 0.038
128
P ATM020 Autoimmune Enteropathy 38 0.038
129
P ADT004 Auditory Neuropathy 37 0.038
130
P THR015 Thrombophilia 59 0.037
131
HMR002 Hemarthrosis 48 0.037
132
LMY002 Leiomyoma 42 0.037
133
P CYS017 Cystic Teratoma 41 0.037
134
LPB001 Lipoblastoma 35 0.037
135
WST001 West Syndrome 61 0.036
136
DBT004 Diabetic Polyneuropathy 51 0.036
137
BRD001 Brody Myopathy 49 0.036
138
SXD001 Sex Differentiation Disease 40 0.036
139
EPD018 Epididymo-Orchitis 31 0.036
140
c HMP004 Hemophilia B 62 0.036
141
INN002 Inner Ear Disease 50 0.036
142
c INT072 Intestinal Pseudo-Obstruction 46 0.036
143
ENT001 Enterocele 41 0.036
144
DLT013 Deletion 5q35 13 0.036
145
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.034
146
MLR007 Male Reproductive System Disease 37 0.034
147
SWL001 Swallowing Disorders 34 0.034
148
IRS003 Iris Disease 32 0.034
149
P SCL047 Sclerocornea 26 0.034
150
c CRN177 Coronary Heart Disease 7 22 0.034