Search results for intu

86 hits were found for intu

# Family MCID Name MIFTS Score
1
c SHR116 Short-Rib Thoracic Dysplasia 20 with Polydactyly 24 30.833
2
c ORF051 Orofaciodigital Syndrome Xvii 22 19.878
3
P PLY006 Polydactyly 59 17.243
4
P ORF001 Orofaciodigital Syndrome 50 15.692
5
SHR044 Short Rib-Polydactyly Syndrome 46 15.260
6
P NPH005 Nephronophthisis 56 14.634
7
ASP005 Asphyxiating Thoracic Dystrophy 47 13.544
8
MHR002 Mohr Syndrome 35 12.226
9
c SHR063 Short-Rib Thoracic Dysplasia 7 with or Without Polydactyly 48 11.164
10
ELL001 Ellis-Van Creveld Syndrome 62 10.715
11
c SHR072 Short-Rib Thoracic Dysplasia 3 with or Without Polydactyly 59 10.715
12
c JVN041 Juvenile Nephronophthisis 43 9.088
13
ACD008 Acid-Labile Subunit Deficiency 52 9.088
14
c JBR025 Joubert Syndrome 17 44 8.961
15
CLF004 Cleft Lip/palate 57 7.577
16
SPN221 Spina Bifida Occulta 40 7.577
17
ACR041 Acromelic Frontonasal Dysostosis 53 7.577
18
SHR098 Short-Rib Thoracic Dysplasia 12 48 7.577
19
VRT007 Vertical Talus, Congenital 51 7.577
20
P MNN007 Meningocele 39 7.577
21
c BSL007 Basal Cell Carcinoma 68 3.271
22
ISC004 Ischemia 61 2.831
23
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 2.569
24
P SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 60 2.137
25
c HRM005 Hermansky-Pudlak Syndrome 1 55 1.384
26
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 1.384
27
c HRM007 Hermansky-Pudlak Syndrome 4 46 1.384
28
P HRM001 Hermansky-Pudlak Syndrome 65 1.384
29
INT051 Intussusception 52 1.199
30
ACT084 Acute Stress Disorder 54 1.199
31
P END044 Endometriosis 62 1.199
32
PST028 Post-Traumatic Stress Disorder 59 1.199
33
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 0.979
34
c ART101 Aortic Valve Disease 2 66 0.874
35
P ART018 Aortic Valve Insufficiency 52 0.874
36
LTR017 Lateral Facial Cleft 11 0.692
37
c ORF037 Orofaciodigital Syndrome I 59 0.692
38
P MCK013 Meckel Syndrome, Type 1 64 0.692
39
SJG002 Sjogren-Larsson Syndrome 54 0.692
40
LPM012 Lipomatosis, Multiple 60 0.692
41
ENL011 Enolase, Sperm Specific 11 0.692
42
ATS010 Autosomal Recessive Disease 42 0.692
43
c SHR066 Short-Rib Thoracic Dysplasia 4 with or Without Polydactyly 45 0.692
44
P URN019 Urinary Tract Infection 49 0.692
45
P PLY014 Polycystic Kidney Disease 69 0.692
46
DDN011 Duodenal Atresia 48 0.692
47
NRL016 Neural Tube Defects 81 0.692
48
P JBR020 Joubert Syndrome 1 74 0.692
49
MYL069 Myeloma, Multiple 77 0.692
50
MCK029 Meckel Diverticulum 38 0.692
51
INF058 Inflammatory Myofibroblastic Tumor 45 0.692
52
MCR103 Microtia 44 0.692
53
FCL090 Facial Cleft 30 0.692
54
P VSC011 Vasculitis 61 0.692
55
P NRP001 Neuropathy 60 0.692
56
NRM005 Neuromuscular Disease 63 0.692
57
ICH043 Ichthyosis, Spastic Quadriplegia, and Mental Retardation 25 0.692
58
PLM005 Pleomorphic Lipoma 40 0.692
59
P HYP086 Hypothyroidism 69 0.692
60
SPS004 Spastic Quadriplegia 40 0.692
61
THY030 Thyroid Gland Disease 50 0.692
62
P PRP019 Peripheral Nervous System Disease 58 0.692
63
PRP030 Purpura 54 0.692
64
QDR001 Quadriplegia 50 0.692
65
P ICH004 Ichthyosis 56 0.692
66
P HYP265 Hypotonia 42 0.692
67
P BRS047 Breast Cancer 98 0.533
68
P PNC035 Pancreatic Cancer 86 0.533
69
P LKM062 Leukemia, Acute Lymphoblastic 69 0.533
70
MYL005 Myelofibrosis 71 0.533
71
P MLN008 Melanoma 76 0.533
72
SML031 Small Cell Carcinoma of the Bladder 46 0.406
73
P BLD134 Bladder Cancer 79 0.406
74
IRN008 Iron Overload in Africa 51 0.406
75
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.406
76
HPT079 Hepatoid Adenocarcinoma 39 0.406
77
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.406
78
RJS001 Ruijs-Aalfs Syndrome 47 0.406
79
c HPT073 Hepatitis C Virus 71 0.406
80
P HPT023 Hepatocellular Carcinoma 96 0.406
81
PDT042 Pediatric Hepatocellular Carcinoma 49 0.406
82
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.406
83
ADL096 Adult Hepatocellular Carcinoma 60 0.406
84
FBR086 Fibrolamellar Carcinoma 59 0.406
85
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.406
86
PTY007 Pityriasis Rotunda 26 0.406
Content
Loading form....