Search results for tyr

125 hits were found for tyr

# Family MCID Name MIFTS Score
1
c ALB009 Albinism, Oculocutaneous, Type Ia 41 4.898
2
ALB002 Albinism 45 4.550
3
c ALB010 Albinism, Oculocutaneous, Type Ib 32 4.309
4
P OCL002 Oculocutaneous Albinism 57 4.217
5
P OCL001 Ocular Albinism 46 3.679
6
P WRD001 Waardenburg's Syndrome 57 3.304
7
P ALB023 Albinism, Ocular, with Sensorineural Deafness 32 3.114
8
c SKN068 Skin/hair/eye Pigmentation, Variation in, 3 23 3.114
9
AML001 Amelanotic Melanoma 42 3.004
10
CHD001 Chediak-Higashi Syndrome 67 2.955
11
SKN019 Skin Melanoma 63 2.955
12
P HRM001 Hermansky-Pudlak Syndrome 62 2.955
13
VGT001 Vogt-Koyanagi-Harada Disease 60 2.955
14
ANG018 Angiomyolipoma 50 2.955
15
MLN008 Melanoma 72 2.697
16
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 2.637
17
c BSL007 Basal Cell Carcinoma 66 2.588
18
P CNG024 Congenital Nystagmus 40 2.588
19
P MLN069 Melanoma, Uveal 63 2.559
20
MCR013 Microphthalmia 61 2.559
21
ATS010 Autosomal Recessive Disease 40 2.559
22
PGM003 Pigmentation Disease 36 2.559
23
STR020 Strabismus 55 2.090
24
c ACT071 Acute Kidney Failure 54 2.090
25
LNT004 Lentigines 52 2.090
26
c DWL002 Dowling-Degos Disease 1 50 2.090
27
DYS022 Dyschromatosis Symmetrica Hereditaria 49 2.090
28
MLN065 Melanocytic Nevus Syndrome, Congenital 49 2.090
29
c HRM005 Hermansky-Pudlak Syndrome 1 47 2.090
30
c HRM006 Hermansky-Pudlak Syndrome 3 47 2.090
31
TTZ003 Tietz Albinism-Deafness Syndrome 44 2.090
32
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 44 2.090
33
P DWL001 Dowling-Degos Disease 43 2.090
34
ACT011 Acute Contagious Conjunctivitis 40 2.090
35
VLV020 Vulvar Melanoma 37 2.090
36
BRS004 Breast Angiosarcoma 36 2.090
37
MLG005 Malignant Spindle Cell Melanoma 35 2.090
38
INT013 Intramuscular Hemangioma 35 2.090
39
ACT003 Acute Kidney Tubular Necrosis 34 2.090
40
HLN001 Halo Nevi 33 2.090
41
P INT283 Integumentary System Cancer 33 2.090
42
MLG007 Malignant Skin Fibrous Histiocytoma 32 2.090
43
CNT041 Central Nervous System Melanocytic Neoplasm 32 2.090
44
MLN005 Melanoacanthoma 30 2.090
45
c MLG063 Malignant Dermis Tumor 28 2.090
46
PGM002 Pigmented Basal Cell Carcinoma 28 2.090
47
KDN001 Kidney Cortex Necrosis 27 2.090
48
MLN009 Melanotic Neurilemmoma 27 2.090
49
DFF013 Diffuse Meningeal Melanocytosis 23 2.090
50
TYR014 Tyrosinase-Like 22 2.090
51
DPN002 Deep Angioma 21 2.090
52
EPT001 Epithelioid Cell Melanoma 20 2.090
53
NCL001 Nuclear Senile Cataract 19 2.090
54
MLG062 Malignant Ciliary Body Melanoma 15 2.090
55
CLR122 Ciliary Body Cancer 12 2.090
56
c ALB025 Albinism, Ocular, with Late-Onset Sensorineural Deafness 26 1.656
57
c ALB024 Albinism, Ocular, Type I 44 1.586
58
MNM005 Minimal Pigment Oculocutaneous Albinism Type 1 9 1.523
59
c CLL013 Cell Type Cancer 37 1.478
60
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.237
61
c BLD140 Blood Group, I System 37 0.121
62
P BRS047 Breast Cancer 100 0.094
63
P PNC044 Pancreatitis 64 0.094
64
P MYC084 Mycobacterium Tuberculosis 1 69 0.077
65
GST050 Gastrointestinal System Disease 66 0.077
66
P THL005 Thalassemia 65 0.077
67
P BRN019 Bernard-Soulier Syndrome 60 0.077
68
PNC034 Pancreas Disease 59 0.077
69
NRN004 Neuroendocrine Tumor 58 0.077
70
EXC002 Exocrine Pancreatic Insufficiency 45 0.077
71
c BSL024 Basal Cell Carcinoma 1 42 0.077
72
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 31 0.077
73
P STR035 Streptococcal Group a Invasive Disease 28 0.077
74
P ALZ034 Alzheimer Disease 95 0.054
75
P PNC035 Pancreatic Cancer 89 0.054
76
ULC004 Ulcerative Colitis 80 0.054
77
P MDL005 Medulloblastoma 76 0.054
78
SQM006 Squamous Cell Carcinoma 74 0.054
79
P NRB001 Neuroblastoma 73 0.054
80
P AMY004 Amyloidosis 69 0.054
81
c MLT160 Multiple Endocrine Neoplasia, Type Iia 65 0.054
82
APP008 Appendicitis 64 0.054
83
P LNG028 Long Qt Syndrome 63 0.054
84
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.054
85
THY111 Thyroid Carcinoma, Familial Medullary 63 0.054
86
CLT003 Colitis 63 0.054
87
P HML002 Hemolytic Anemia 62 0.054
88
P FBR017 Fibrosarcoma 61 0.054
89
P MLG056 Malignant Hyperthermia 60 0.054
90
c ALP101 Alpha-Thalassemia 60 0.054
91
PRS047 Prostatitis 59 0.054
92
ORL015 Oral Squamous Cell Carcinoma 59 0.054
93
P LPR002 Leopard Syndrome 56 0.054
94
P ACT008 Actinic Keratosis 56 0.054
95
P THY032 Thyroiditis 56 0.054
96
P MLT074 Multiple Endocrine Neoplasia 55 0.054
97
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 55 0.054
98
P HYP750 Hypertriglyceridemia, Familial 55 0.054
99
P HMG032 Hemoglobin H Disease 53 0.054
100
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 53 0.054
101
KRT009 Keratosis 53 0.054
102
EWN002 Ewing's Family of Tumors 49 0.054
103
PRT011 Protein C Deficiency 48 0.054
104
P MTH007 Methemoglobinemia 46 0.054
105
END072 Endotheliitis 46 0.054
106
PRC038 Precocious Puberty, Male-Limited 46 0.054
107
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.054
108
PHC013 Phaeochromocytoma 44 0.054
109
MRP001 Morphine Dependence 43 0.054
110
HYP141 Hyperphenylalaninemia 43 0.054
111
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 41 0.054
112
PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 40 0.054
113
MTH064 Methemoglobinemia, Beta-Globin Type 38 0.054
114
DLT018 Dilution, Pigmentary 37 0.054
115
c DYS165 Dysfibrinogenemia, Congenital 37 0.054
116
PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 36 0.054
117
PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 35 0.054
118
PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 35 0.054
119
c HNT011 Huntington Disease-Like 3 35 0.054
120
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.054
121
LCH014 Lichen Amyloidosis 33 0.054
122
c CNG223 Congenital Methemoglobinemia 30 0.054
123
P RNG031 Ring Chromosome Y Syndrome 29 0.054
124
TST023 Testotoxicosis 27 0.054
125
CHL098 Childhood Myocerebrohepatopathy Spectrum 15 0.054
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