Search results for tyr

100 hits were found for tyr

# Family MCID Name MIFTS Score
1
c ALB009 Albinism, Oculocutaneous, Type Ia 37 5.058
2
ALB002 Albinism 45 4.698
3
P OCL002 Oculocutaneous Albinism 55 4.352
4
c ALB010 Albinism, Oculocutaneous, Type Ib 32 4.147
5
OCL001 Ocular Albinism 43 3.787
6
P WRD001 Waardenburg's Syndrome 56 3.399
7
AML001 Amelanotic Melanoma 37 3.092
8
CHD001 Chediak-Higashi Syndrome 65 3.040
9
SKN019 Skin Melanoma 61 3.040
10
P HRM001 Hermansky-Pudlak Syndrome 61 3.040
11
P UVL004 Uveal Melanoma 60 3.040
12
VGT001 Vogt-Koyanagi-Harada Disease 55 3.040
13
ANG018 Angiomyolipoma 45 3.040
14
MLN008 Melanoma 70 2.781
15
WRD021 Waardenburg Syndrome/ocular Albinism, Digenic 32 2.716
16
P CNG024 Congenital Nystagmus 39 2.664
17
MCR013 Microphthalmia 59 2.633
18
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 51 2.633
19
ATS010 Autosomal Recessive Disease 39 2.633
20
PGM003 Pigmentation Disease 39 2.633
21
P MLN043 Melanoma, Cutaneous Malignant 8 36 2.218
22
c HRM005 Hermansky-Pudlak Syndrome 1 52 2.150
23
P STR020 Strabismus 52 2.150
24
c HRM006 Hermansky-Pudlak Syndrome 3 49 2.150
25
c ACT071 Acute Kidney Failure 48 2.150
26
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 46 2.150
27
DYS022 Dyschromatosis Symmetrica Hereditaria 46 2.150
28
TTZ003 Tietz Albinism-Deafness Syndrome 41 2.150
29
P DWL001 Dowling-Degos Disease 41 2.150
30
c DWL002 Dowling-Degos Disease 1 41 2.150
31
VLV020 Vulvar Melanoma 38 2.150
32
BRS004 Breast Angiosarcoma 36 2.150
33
ACT011 Acute Contagious Conjunctivitis 35 2.150
34
CNT041 Central Nervous System Melanocytic Neoplasm 33 2.150
35
INT013 Intramuscular Hemangioma 32 2.150
36
MLG007 Malignant Skin Fibrous Histiocytoma 31 2.150
37
MLG005 Malignant Spindle Cell Melanoma 30 2.150
38
P INT283 Integumentary System Cancer 30 2.150
39
c MLG063 Malignant Dermis Tumor 29 2.150
40
ACT003 Acute Kidney Tubular Necrosis 29 2.150
41
MLN005 Melanoacanthoma 27 2.150
42
PGM002 Pigmented Basal Cell Carcinoma 27 2.150
43
KDN001 Kidney Cortex Necrosis 26 2.150
44
HLN001 Halo Nevi 25 2.150
45
NCL001 Nuclear Senile Cataract 22 2.150
46
EPT001 Epithelioid Cell Melanoma 22 2.150
47
DPN002 Deep Angioma 21 2.150
48
CLR122 Ciliary Body Cancer 21 2.150
49
MLN009 Melanotic Neurilemmoma 20 2.150
50
DFF013 Diffuse Meningeal Melanocytosis 20 2.150
51
MLG062 Malignant Ciliary Body Melanoma 17 2.150
52
OCL046 Ocular Albinism, Type I, Nettleship-Falls Type 34 1.637
53
MNM005 Minimal Pigment Oculocutaneous Albinism Type 1 9 1.568
54
c CLL013 Cell Type Cancer 48 1.520
55
P BRS047 Breast Cancer 100 0.101
56
P PNC044 Pancreatitis 60 0.101
57
TBR010 Tuberculosis 69 0.082
58
P THL005 Thalassemia 61 0.082
59
PNC034 Pancreas Disease 55 0.082
60
NRN004 Neuroendocrine Tumor 55 0.082
61
GST050 Gastrointestinal System Disease 53 0.082
62
EXC002 Exocrine Pancreatic Insufficiency 42 0.082
63
P PNC035 Pancreatic Cancer 84 0.058
64
P MDL005 Medulloblastoma 73 0.058
65
ULC004 Ulcerative Colitis 72 0.058
66
P NRB001 Neuroblastoma 71 0.058
67
SQM006 Squamous Cell Carcinoma 69 0.058
68
P ADN016 Adenocarcinoma 69 0.058
69
P LNG028 Long Qt Syndrome 64 0.058
70
P AMY004 Amyloidosis 64 0.058
71
c BSL007 Basal Cell Carcinoma 64 0.058
72
P HYP117 Hypertriglyceridemia 61 0.058
73
P HML002 Hemolytic Anemia 61 0.058
74
APP008 Appendicitis 59 0.058
75
CLT003 Colitis 58 0.058
76
RBS003 Rabson-Mendenhall Syndrome 57 0.058
77
MLG056 Malignant Hyperthermia 57 0.058
78
CRN183 Carnitine Palmitoyltransferase Ii Deficiency 56 0.058
79
ORL015 Oral Squamous Cell Carcinoma 55 0.058
80
PRS047 Prostatitis 55 0.058
81
P FBR017 Fibrosarcoma 54 0.058
82
P LPR002 Leopard Syndrome 54 0.058
83
P MLT074 Multiple Endocrine Neoplasia 54 0.058
84
P THY032 Thyroiditis 53 0.058
85
ACT008 Actinic Keratosis 51 0.058
86
PRT011 Protein C Deficiency 49 0.058
87
KRT009 Keratosis 48 0.058
88
HYP141 Hyperphenylalaninemia 48 0.058
89
c BSL024 Basal Cell Carcinoma 1 45 0.058
90
P MTH007 Methemoglobinemia 44 0.058
91
c CHR095 Chronic Progressive External Ophthalmoplegia 43 0.058
92
MRP001 Morphine Dependence 42 0.058
93
END072 Endotheliitis 41 0.058
94
PHC013 Phaeochromocytoma 41 0.058
95
GRM001 Germ Cell and Embryonal Cancer 38 0.058
96
P GRM010 Germ Cells Tumors 34 0.058
97
LCH014 Lichen Amyloidosis 30 0.058
98
TST023 Testotoxicosis 27 0.058
99
c CNG223 Congenital Methemoglobinemia 26 0.058
100
OCL012 Ocular Albinism with Sensorineural Deafness 22 0.058
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