Search results for "[genes] NTRK1"

34 hits were found for '[genes] NTRK1'

# Family MCID Name MIFTS Score
1
THY028 Thyroid Cancer 69 20.719
2
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 32 20.719
3
P MDL022 Medullary Thyroid Carcinoma, Familial 63 19.381
4
ANH002 Anhidrosis 41 19.381
5
DBT010 Diabetic Neuropathy 55 16.380
6
THY103 Thyroid Cancer, Monmedullary, 1 53 16.380
7
GNG002 Ganglioneuroma 47 16.380
8
ATN004 Autonomic Neuropathy 45 16.380
9
OLF005 Olfactory Neuroblastoma 44 16.380
10
GNG008 Ganglioneuroblastoma 40 16.380
11
P ALZ034 Alzheimer Disease 92 14.651
12
P MDL005 Medulloblastoma 77 14.651
13
CHG001 Chagas Disease 67 14.651
14
P HRD021 Hereditary Sensory Neuropathy 46 14.651
15
P NRX001 Neuroaxonal Dystrophy 38 14.651
16
ASK001 Askin's Tumor 29 14.651
17
P PHC003 Pheochromocytoma 71 12.688
18
P NRB001 Neuroblastoma 70 12.688
19
PYR013 Pyruvate Kinase Deficiency 58 12.688
20
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 54 12.688
21
OCL020 Ocular Cicatricial Pemphigoid 52 12.688
22
c SPN314 Spinocerebellar Ataxia 10 49 12.688
23
PRP021 Peripheral Nervous System Neoplasm 46 12.688
24
ATN003 Autonomic Nervous System Neoplasm 40 12.688
25
PRL010 Prolactin Producing Pituitary Tumor 38 12.688
26
P LTH016 Lethal Congenital Contractural Syndrome 2 36 12.688
27
SWT003 Sweat Gland Disease 34 12.688
28
CNJ017 Conjunctival Nevus 29 12.688
29
FML143 Familial Papillary Thyroid Carcinoma 28 12.688
30
c NTR012 Ntrk1-Related Familial Medullary Thyroid Carcinoma 7 12.688
31
P NRV006 Nervous System Cancer 60 10.360
32
DFF036 Differentiated Thyroid Carcinoma 50 10.360
33
P CRB102 Cerebral Cavernous Malformations-2 46 10.360
34
c CHR530 Charcot-Marie-Tooth Disease, Type 2b 40 10.360