NGF, nerve growth factor, 4803

N. diseases: 616; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		0.800 CausalMutation disease CLINVAR
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		0.800 Biomarker disease CTD_human
CUI: C0020074
Disease: HSAN Type IV
HSAN Type IV 		0.400 Biomarker disease CTD_human
CUI: C0027889
Disease: Hereditary Sensory and Autonomic Neuropathies
Hereditary Sensory and Autonomic Neuropathies 		0.330 Biomarker group CTD_human
CUI: C0699739
Disease: Sensory Neuropathy, Hereditary
Sensory Neuropathy, Hereditary 		0.320 Biomarker disease CTD_human
CUI: C0020071
Disease: Hereditary Sensory Autonomic Neuropathy, Type 1
Hereditary Sensory Autonomic Neuropathy, Type 1 		0.300 Biomarker disease CTD_human
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		0.300 Biomarker disease CTD_human
CUI: C0086405
Disease: Hereditary Sensory Radicular Neuropathy
Hereditary Sensory Radicular Neuropathy 		0.300 Biomarker disease CTD_human
CUI: C0003028
Disease: Anhidrosis
Anhidrosis 		0.150 Biomarker disease HPO
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		0.100 Biomarker disease HPO
CUI: C0029443
Disease: Osteomyelitis
Osteomyelitis 		0.100 Biomarker disease HPO
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition 		0.100 Biomarker phenotype HPO
CUI: C0344307
Disease: Absence of pain sensation
Absence of pain sensation 		0.100 Biomarker phenotype HPO
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		0.100 Biomarker phenotype HPO
CUI: C1837522
Disease: Impaired pain sensation
Impaired pain sensation 		0.100 Biomarker phenotype HPO
CUI: C1837602
Disease: Painless fractures due to injury
Painless fractures due to injury 		0.100 Biomarker phenotype HPO
CUI: C1851789
Disease: Poor wound healing
Poor wound healing 		0.100 Biomarker phenotype HPO
CUI: C1858085
Disease: Malar flattening
Malar flattening 		0.100 Biomarker disease HPO
CUI: C4021222
Disease: Impaired temperature sensation
Impaired temperature sensation 		0.100 Biomarker disease HPO
CUI: C4021816
Disease: Abnormality of the gingiva
Abnormality of the gingiva 		0.100 Biomarker disease HPO
CUI: C4024916
Disease: Decreased number of small peripheral myelinated nerve fibers
Decreased number of small peripheral myelinated nerve fibers 		0.100 Biomarker phenotype HPO
CUI: C4732740
Disease: Acral ulceration
Acral ulceration 		0.100 Biomarker phenotype HPO
CUI: C0238462
Disease: Medullary carcinoma of thyroid
Medullary carcinoma of thyroid 		0.010 AlteredExpression disease BEFREE High level of a nerve growth factor in the serum of a patient with medullary carcinoma of the thyroid gland. 844218 1977
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		0.010 AlteredExpression disease BEFREE The serum of a patient with a familial medullary thyroid carcinoma showed levels of a factor, active in the nerve growth factor (NGF) bioassay and cross-reacting immunologically with mouse NGF, 20-1000 times higher than sera from normal controls or from patients with unrelated tumours. 844218 1977
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1 		0.030 GeneticVariation disease BEFREE Central and peripheral forms of neurofibromatosis are closely related but discrete diseases which appear to have separate alterations in nerve growth factor activity. 6774282 1980