Search results for "isolated anorectal malformation"

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

139 hits were found for 'isolated anorectal malformation'

# Family MCID Name MIFTS Score
1
ISL029 Isolated Anorectal Malformation 5 2.350
2
CRB009 Cerebritis 36 0.187
3
IMP002 Imperforate Anus 54 0.182
4
MLN008 Melanoma 61 0.175
5
FCL044 Fecal Incontinence 34 0.142
6
P ADN016 Adenocarcinoma 69 0.140
7
GRW007 Growth Hormone Deficiency 49 0.135
8
CNS004 Constipation 57 0.134
9
URT001 Urethritis 39 0.129
10
BRT030 Birth Defects 44 0.118
11
RCT017 Rectal Disease 35 0.112
12
ACR041 Acromelic Frontonasal Dysostosis 45 0.112
13
NRN002 Neuronitis 40 0.111
14
VGN023 Vaginitis 41 0.110
15
P LKM002 Leukemia 70 0.109
16
P ESP024 Esophagitis 62 0.108
17
ALR002 Al-Raqad Syndrome 36 0.101
18
P TRT010 Teratoma 49 0.101
19
SRC014 Sarcoma 66 0.098
20
P LYM118 Lymphoma 68 0.098
21
SPL040 Split Hand 35 0.096
22
VND001 Vein Disease 51 0.093
23
ANS012 Anus Disease 32 0.093
24
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.090
25
P INT068 Intestinal Disease 60 0.089
26
ADN018 Adenoma 59 0.089
27
P HYP040 Hypospadias 58 0.088
28
PRS047 Prostatitis 56 0.087
29
ESP020 Esophageal Atresia 48 0.086
30
DDN006 Duodenitis 44 0.086
31
P CNG015 Congenital Diaphragmatic Hernia 58 0.085
32
P PLM037 Pulmonary Hypertension 78 0.084
33
P HRT032 Heart Disease 64 0.084
34
c CNG401 Congenital Heart Disease 67 0.084
35
P SPL037 Split Hand Foot Malformation 35 0.084
36
CLN019 Colonic Disease 50 0.081
37
MCN001 Mucinous Adenocarcinoma 48 0.080
38
P NRP001 Neuropathy 57 0.080
39
CYS001 Cystic Fibrosis 87 0.078
40
P MCR010 Microcephaly 60 0.078
41
RCT011 Rectal Prolapse 41 0.077
42
P ART022 Arthritis 73 0.077
43
GST050 Gastrointestinal System Disease 58 0.077
44
ANR002 Aniridia 62 0.075
45
CHL123 Chlamydia 60 0.075
46
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.072
47
EPD016 Epidermolysis Bullosa 59 0.072
48
P PLY006 Polydactyly 56 0.070
49
ORC001 Orchitis 35 0.070
50
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.070
51
P KDN018 Kidney Disease 64 0.070
52
MGC001 Megacolon 50 0.069
53
CLN022 Colonic Atresia 23 0.069
54
P END047 Endophthalmitis 46 0.068
55
SCR024 Sacrococcygeal Teratoma 25 0.067
56
SNS001 Sensorineural Hearing Loss 52 0.067
57
P PYL005 Pyelonephritis 52 0.064
58
P CTR002 Cataract 57 0.064
59
CLT003 Colitis 56 0.064
60
P ENC008 Encephalocele 48 0.063
61
FNC005 Functional Colonic Disease 32 0.062
62
CTY001 Cat Eye Syndrome 42 0.062
63
c BRN108 Branchiootic Syndrome 1 36 0.062
64
KDS001 Kid Syndrome 53 0.061
65
INT060 Intestinal Atresia 37 0.061
66
PRD011 Proud Syndrome 42 0.061
67
P KLP003 Klippel-Feil Syndrome 47 0.061
68
P NRV007 Nervous System Disease 71 0.061
69
P HRS035 Hirschsprung Disease 1 58 0.060
70
VHW001 Vohwinkel Syndrome 47 0.060
71
PTR006 Peters Anomaly 64 0.060
72
P BLD051 Blood Coagulation Disease 44 0.059
73
GST019 Gastrointestinal Stromal Tumor 73 0.059
74
P HMP007 Hemophilia 55 0.059
75
ACQ007 Acquired Immunodeficiency Syndrome 60 0.059
76
ADT003 Auditory System Disease 49 0.058
77
DMY004 Demyelinating Disease 52 0.058
78
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.058
79
SPN041 Spinal Cord Disease 50 0.058
80
SKN016 Skin Disease 69 0.058
81
P OBS005 Obesity 91 0.057
82
P ART023 Arthropathy 63 0.056
83
c HYP595 Hypertension, Essential 69 0.056
84
NRL016 Neural Tube Defects 76 0.056
85
CRD001 Cardiac Tamponade 43 0.055
86
P SYP003 Syphilis 51 0.055
87
GLB003 Globe Disease 34 0.055
88
DYS073 Dysphagia 51 0.055
89
DWN001 Down Syndrome 65 0.054
90
c PTS008 Ptosis, Congenital 29 0.054
91
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 43 0.054
92
ADL002 Adult Syndrome 53 0.054
93
P DNR001 Duane Retraction Syndrome 41 0.053
94
c CRN214 Coronary Heart Disease 5 22 0.052
95
HMR002 Hemarthrosis 47 0.052
96
CNG069 Congenital Cytomegalovirus 34 0.051
97
c INH004 Inherited Blood Coagulation Disease 38 0.051
98
CHN016 Cohen Syndrome 55 0.050
99
P ADT004 Auditory Neuropathy 36 0.050
100
c CNG031 Congenital Nervous System Abnormality 39 0.050
101
VSC007 Vascular Disease 51 0.050
102
SKN023 Skin Tag 48 0.050
103
SXL003 Sexual Disorder 45 0.050
104
DLT013 Deletion 5q35 13 0.050
105
P PFF001 Pfeiffer Syndrome 73 0.050
106
P MNC007 Monocytic Leukemia 52 0.049
107
NRG002 Neurogenic Bladder 47 0.048
108
P JVN008 Juvenile Glaucoma 33 0.048
109
P DYS007 Dyskeratosis Congenita 64 0.048
110
c PST041 Posterior Urethral Valves 46 0.048
111
INN002 Inner Ear Disease 48 0.047
112
INT067 Interstitial Nephritis 48 0.047
113
VCT001 Vacterl Association 47 0.047
114
OCC011 Occipital Encephalocele 24 0.046
115
SXD001 Sex Differentiation Disease 39 0.046
116
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.046
117
P PLN008 Peeling Skin Syndrome 45 0.046
118
SYS003 Systolic Heart Failure 42 0.046
119
c HMP004 Hemophilia B 61 0.046
120
SPC003 Specific Developmental Disorder 39 0.044
121
ESP023 Esophageal Disease 52 0.044
122
NSL022 Nasal Cavity Disease 41 0.044
123
P ATM020 Autoimmune Enteropathy 37 0.043
124
DDN011 Duodenal Atresia 40 0.043
125
VTR016 Vater/vacterl Association 37 0.043
126
LMY002 Leiomyoma 56 0.040
127
P CYS017 Cystic Teratoma 40 0.040
128
SPN186 Spinal Cord Injury 62 0.039
129
PNL023 Penile Agenesis 21 0.039
130
LPB001 Lipoblastoma 35 0.039
131
BRD001 Brody Myopathy 49 0.039
132
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.039
133
ENT001 Enterocele 39 0.038
134
EPD018 Epididymo-Orchitis 32 0.037
135
c INT072 Intestinal Pseudo-Obstruction 45 0.036
136
WST001 West Syndrome 61 0.034
137
MLR007 Male Reproductive System Disease 36 0.034
138
SWL001 Swallowing Disorders 33 0.034
139
c CRN177 Coronary Heart Disease 7 21 0.034