Search results for ednrb

115 hits were found for ednrb

# Family MCID Name MIFTS Score
1
c HRS036 Hirschsprung Disease 2 36 5.692
2
c WRD020 Waardenburg Syndrome, Type 4a 48 4.505
3
P WRD001 Waardenburg's Syndrome 59 4.070
4
ABC001 Abcd Syndrome 41 3.976
5
P HRS035 Hirschsprung Disease 1 65 3.306
6
P PRS040 Prostate Cancer 97 3.242
7
P HRT032 Heart Disease 75 2.878
8
P PLM037 Pulmonary Hypertension 67 2.878
9
c HYP595 Hypertension, Essential 84 2.493
10
CRV035 Cervical Cancer 76 2.493
11
P KDN018 Kidney Disease 72 2.493
12
c WRD030 Waardenburg Syndrome, Type 1 56 2.347
13
P INT070 Intestinal Obstruction 58 2.129
14
CNS004 Constipation 58 2.129
15
c WRD032 Waardenburg Syndrome, Type 2a 46 2.129
16
RRG078 Rare Genetic Deafness 29 2.129
17
MGC001 Megacolon 46 2.102
18
c MGR028 Migraine with or Without Aura 1 67 2.071
19
c WRD033 Waardenburg Syndrome, Type 2e 53 2.071
20
P MGR003 Migraine with Aura 52 2.071
21
STR067 Stroke, Ischemic 81 2.035
22
c DLT002 Dilated Cardiomyopathy 79 2.035
23
CNT097 Central Hypoventilation Syndrome, Congenital 71 2.035
24
CNN005 Connective Tissue Disease 68 2.035
25
P OLG002 Oligodendroglioma 67 2.035
26
LBR036 Leber Plus Disease 66 2.035
27
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 2.035
28
P VSC007 Vascular Disease 63 2.035
29
INT323 Intraocular Pressure Quantitative Trait Locus 62 2.035
30
P OPT006 Optic Nerve Disease 60 2.035
31
PRT013 Portal Hypertension 59 2.035
32
P MCR010 Microcephaly 59 2.035
33
P CYS039 Cystic Kidney Disease 54 2.035
34
P ORL007 Oral Cavity Cancer 53 2.035
35
IMP005 Impotence 52 2.035
36
GNG012 Gingival Overgrowth 51 2.035
37
HPT009 Hepatopulmonary Syndrome 48 2.035
38
GLD006 Goldberg-Shprintzen Syndrome 47 2.035
39
RTT001 Ritter's Disease 41 2.035
40
SCR015 Scarlet Fever 39 2.035
41
ACT040 Acute Poststreptococcal Glomerulonephritis 36 2.035
42
AGN004 Aganglionosis, Total Intestinal 22 1.580
43
c WRD010 Waardenburg Syndrome Type 4 29 1.523
44
CFF002 Coffin-Lowry Syndrome 60 1.486
45
PBL005 Piebald Trait 59 1.486
46
TTZ003 Tietz Albinism-Deafness Syndrome 58 1.486
47
c DPH024 Diaphragmatic Hernia, Congenital 63 1.439
48
PRP066 Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease 51 1.439
49
LNT004 Lentigines 50 1.439
50
PYD002 Pyoderma 50 1.439
51
IMP004 Impetigo 49 1.439
52
MLT006 Multidrug-Resistant Tuberculosis 48 1.439
53
RDT013 Radiation Proctitis 47 1.439
54
c WRD019 Waardenburg Syndrome, Type 4b 45 1.439
55
c WRD031 Waardenburg Syndrome, Type 3 45 1.439
56
c WRD024 Waardenburg Syndrome, Type 4c 45 1.439
57
c CHR096 Chronic Pulmonary Heart Disease 43 1.439
58
PYM001 Pyomyositis 41 1.439
59
ORL003 Oral Tuberculosis 39 1.439
60
P INT260 Intracranial Berry Aneurysm 39 1.439
61
BLL012 Bullous Impetigo 39 1.439
62
c BRC080 Brachydactyly, Type A1, B 38 1.439
63
c WRD022 Waardenburg Syndrome, Type 2d 35 1.439
64
c SPN419 Spinocerebellar Ataxia 45 35 1.439
65
c MLG003 Malignant Renovascular Hypertension 32 1.439
66
c WRD026 Waardenburg Syndrome, Type 2c 29 1.439
67
CMM006 Commensal Bacterial Infectious Disease 27 1.439
68
CCH001 Cochlear Disease 26 1.439
69
PLM189 Pulmonary Arterial Hypertension Associated with Connective Tissue Disease 26 1.439
70
TRN011 Transient Refractive Change 25 1.439
71
DBL001 Double Pterygium 9 1.439
72
c BRN108 Branchiootic Syndrome 1 62 0.114
73
P LNG032 Lung Cancer 98 0.081
74
P BLD134 Bladder Cancer 79 0.081
75
ADN011 Adenoid Cystic Carcinoma 70 0.081
76
P NSP012 Nasopharyngeal Carcinoma 66 0.081
77
SQM006 Squamous Cell Carcinoma 60 0.081
78
P SNS001 Sensorineural Hearing Loss 60 0.081
79
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.081
80
P HPT023 Hepatocellular Carcinoma 100 0.057
81
P CLR023 Colorectal Cancer 99 0.057
82
P ALZ034 Alzheimer Disease 88 0.057
83
c LKM061 Leukemia, Acute Myeloid 84 0.057
84
P GST053 Gastric Cancer 83 0.057
85
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.057
86
P LNG064 Lung Cancer Susceptibility 3 78 0.057
87
END057 Endometrial Cancer 74 0.057
88
c LKM063 Leukemia, Chronic Myeloid 72 0.057
89
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.057
90
P MLN008 Melanoma 69 0.057
91
P LKM062 Leukemia, Acute Lymphoblastic 69 0.057
92
P LKM002 Leukemia 68 0.057
93
P MCR115 Microvascular Complications of Diabetes 5 66 0.057
94
P ADN016 Adenocarcinoma 64 0.057
95
P GLM045 Glioma 63 0.057
96
P MYL006 Myeloid Leukemia 60 0.057
97
ORL011 Oral Cancer 60 0.057
98
c DWL002 Dowling-Degos Disease 1 58 0.057
99
LYM027 Lymphopenia 58 0.057
100
CLR030 Clear Cell Renal Cell Carcinoma 53 0.057
101
HYP748 Hypertelorism 50 0.057
102
PRS129 Prostatic Hyperplasia, Benign 49 0.057
103
ATS010 Autosomal Recessive Disease 48 0.057
104
ALB002 Albinism 46 0.057
105
CHR492 Chromosome 13q14 Deletion Syndrome 46 0.057
106
GLL048 Glial Tumor 45 0.057
107
NSP002 Nasopharyngitis 43 0.057
108
ORL015 Oral Squamous Cell Carcinoma 43 0.057
109
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.057
110
CRN264 Craniosynostosis with Fibular Aplasia 29 0.057
111
HYP572 Hypoganglionosis 28 0.057
112
c HRS029 Hirschsprung Disease 4 24 0.057
113
HTR005 Heterochromia Iridis 22 0.057
114
CTT001 Catatrichy 15 0.057
115
c HRS025 Hirschsprung Disease 8 14 0.057
Content
Loading form....