Search results for ntrk1

121 hits were found for ntrk1

# Family MCID Name MIFTS Score
1
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 54 5.764
2
P BRS047 Breast Cancer 96 4.018
3
ANH002 Anhidrosis 46 3.938
4
CHR687 Charcot-Marie-Tooth Disease/hereditary Motor and Sensory Neuropathy 40 3.857
5
THY111 Thyroid Carcinoma, Familial Medullary 67 3.779
6
ATN004 Autonomic Neuropathy 44 3.428
7
P LNG032 Lung Cancer 97 3.228
8
P PRS040 Prostate Cancer 97 3.185
9
P CHR071 Charcot-Marie-Tooth Disease 64 3.160
10
P NRP001 Neuropathy 56 2.959
11
P OVR042 Ovarian Cancer 89 2.854
12
P PNC035 Pancreatic Cancer 84 2.854
13
P HRD021 Hereditary Sensory Neuropathy 47 2.796
14
THY029 Thyroid Carcinoma 59 2.692
15
PPL002 Papillary Carcinoma 47 2.506
16
THY122 Thyroid Gland Cancer 58 2.479
17
ESP021 Esophageal Cancer 90 2.449
18
P ALZ034 Alzheimer Disease 88 2.449
19
P MDL005 Medulloblastoma 77 2.449
20
P SCH015 Schizophrenia 75 2.449
21
P PHC003 Pheochromocytoma 71 2.449
22
ADN011 Adenoid Cystic Carcinoma 70 2.449
23
CRT072 Creutzfeldt-Jakob Disease 69 2.449
24
CHG001 Chagas Disease 66 2.449
25
GNG002 Ganglioneuroma 53 2.449
26
OLF005 Olfactory Neuroblastoma 49 2.449
27
GNG008 Ganglioneuroblastoma 47 2.449
28
P NRB001 Neuroblastoma 71 2.160
29
P HRS035 Hirschsprung Disease 1 65 2.066
30
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 56 2.066
31
SNS003 Sensory Peripheral Neuropathy 53 2.066
32
P MST009 Mastocytosis 63 2.035
33
FLL031 Follicular Adenoma 39 2.035
34
c AMY091 Amyotrophic Lateral Sclerosis 1 89 1.999
35
c LKM063 Leukemia, Chronic Myeloid 71 1.999
36
PNC129 Pancreatic Adenocarcinoma 67 1.999
37
P OLG002 Oligodendroglioma 67 1.999
38
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 1.999
39
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 66 1.999
40
P ATT013 Attention Deficit-Hyperactivity Disorder 64 1.999
41
INT323 Intraocular Pressure Quantitative Trait Locus 62 1.999
42
DBT010 Diabetic Neuropathy 55 1.999
43
PYL006 Pyloric Stenosis 48 1.999
44
P HYP009 Hypertrophic Pyloric Stenosis 42 1.999
45
ASK001 Askin's Tumor 36 1.999
46
P LNG064 Lung Cancer Susceptibility 3 77 1.461
47
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 1.461
48
DFF036 Differentiated Thyroid Carcinoma 51 1.461
49
THY125 Thyroid Gland Medullary Carcinoma 51 1.461
50
MSN004 Mesenchymal Cell Neoplasm 41 1.461
51
c LKM061 Leukemia, Acute Myeloid 83 1.414
52
P RTN008 Retinitis Pigmentosa 77 1.414
53
RNL065 Renal Cell Carcinoma, Papillary, 1 73 1.414
54
P KBK002 Kabuki Syndrome 1 67 1.414
55
UND005 Undifferentiated Pleomorphic Sarcoma 66 1.414
56
c MLT159 Multiple Endocrine Neoplasia, Type Iib 59 1.414
57
P PRP019 Peripheral Nervous System Disease 57 1.414
58
OCL020 Ocular Cicatricial Pemphigoid 54 1.414
59
THY123 Thyroid Gland Follicular Carcinoma 48 1.414
60
MGC001 Megacolon 46 1.414
61
c NRP044 Neuropathy, Hereditary Sensory and Autonomic, Type Viii 44 1.414
62
c CNG023 Congenital Fibrosarcoma 41 1.414
63
c CNG029 Congenital Mesoblastic Nephroma 40 1.414
64
P PRP021 Peripheral Nervous System Neoplasm 39 1.414
65
CPL002 Capillary Lymphangioma 38 1.414
66
UTR042 Uterus Leiomyosarcoma 38 1.414
67
c SPN326 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2 37 1.414
68
UTR037 Uterine Corpus Sarcoma 36 1.414
69
c BNG029 Benign Struma Ovarii 34 1.414
70
SWT003 Sweat Gland Disease 33 1.414
71
PDT019 Pediatric Fibrosarcoma 30 1.414
72
c ATN017 Autonomic Nervous System Benign Neoplasm 28 1.414
73
TLL001 Tall Cell Variant Papillary Carcinoma 27 1.414
74
P ATN003 Autonomic Nervous System Neoplasm 27 1.414
75
c PRP105 Peripheral Nervous System Benign Neoplasm 26 1.414
76
MLT011 Multiple Mucosal Neuroma 24 1.414
77
DDN022 Duodenum Adenoma 21 1.414
78
CRT003 Cortical Senile Cataract 21 1.414
79
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.345
80
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.241
81
ATS010 Autosomal Recessive Disease 48 0.220
82
THY124 Thyroid Gland Papillary Carcinoma 52 0.180
83
P CLR023 Colorectal Cancer 98 0.150
84
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.080
85
P ART023 Arthropathy 62 0.080
86
DNT012 Dental Caries 51 0.080
87
SPN032 Spindle Cell Carcinoma 45 0.080
88
GLB015 Glioblastoma Multiforme 75 0.057
89
c THR092 Thrombophilia Due to Thrombin Defect 73 0.057
90
MLN008 Melanoma 69 0.057
91
SKN019 Skin Melanoma 67 0.057
92
P SKN015 Skin Carcinoma 67 0.057
93
c SML038 Small Cell Cancer of the Lung 65 0.057
94
CLF027 Cleft Palate, Isolated 64 0.057
95
OST017 Osteomyelitis 64 0.057
96
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.057
97
ADN018 Adenoma 58 0.057
98
CMP010 Complex Regional Pain Syndrome 58 0.057
99
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.057
100
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.057
101
P PLY019 Polyneuropathy 56 0.057
102
P INF049 Infantile Myofibromatosis 55 0.057
103
KRT009 Keratosis 53 0.057
104
P PTS002 Ptosis 52 0.057
105
THR004 Thrombocytosis 51 0.057
106
SPN035 Spindle Cell Sarcoma 51 0.057
107
CLR109 Colorectal Adenocarcinoma 50 0.057
108
BNR002 Bone Resorption Disease 48 0.057
109
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.057
110
ATN005 Autonomic Dysfunction 47 0.057
111
FBR019 Fibromatosis 44 0.057
112
c NRP033 Neuropathy, Hereditary Sensory and Autonomic, Type Ia 43 0.057
113
c HRD201 Hereditary Sensory and Autonomic Neuropathy Type 1 41 0.057
114
HRN029 Hearing Loss, Noise-Induced 37 0.057
115
SPT007 Spitz Nevus 35 0.057
116
c PRS136 Prostate Cancer, Hereditary, 6 33 0.057
117
c PRS130 Prostate Cancer, Hereditary, 8 32 0.057
118
MYP064 Myopericytoma 30 0.057
119
SPT022 Spitzoid Melanoma 29 0.057
120
HYP144 Hyperacusis 23 0.057
121
PTR034 Paternal Uniparental Disomy 23 0.057
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