Diseases Associated With Global Genome Nucleotide-Excision Repair
Disease |
Stomach Neoplasms
|
Peripheral Neuropathy
|
Micronuclei, Chromosome-Defective
|
Prostatic Neoplasms
|
Arsenic Poisoning
|
Toxic Epidermal Necrolysis
|
Neoplasms, Germ Cell And Embryonal
|
Skin Neoplasms
|
Lung Adenocarcinoma
|
Neoplasm Metastasis
|
Genetic Predisposition To Disease
|
Testicular Neoplasms
|
Urinary Bladder Neoplasms
|
Chromosome Aberrations
|
Cardiomyopathies
|
Cerebrooculofacioskeletal Syndrome 2
|
Cerebrooculofacioskeletal Syndrome 4
|
Ceroid Lipofuscinosis, Neuronal 1, Infantile
|
Cleft Lip
|
Cleft Palate
|
Colorectal Cancer
|
Craniofacial Abnormalities
|
Dermatitis
|
Disease Progression
|
Embryo Loss
|
Hepatitis
|
Hyperkeratosis, Epidermolytic
|
Male Infertility
|
Inflammation
|
Intellectual Disability
|
Intestinal Neoplasms
|
Kidney Disease
|
Kyphosis
|
Lung Neoplasms
|
Mammary Neoplasms, Animal
|
Mammary Neoplasms, Experimental
|
Melanoma
|
Mesothelioma, Malignant
|
Multiple Myeloma
|
Nasopharyngeal Carcinoma
|
Neoplasm Invasiveness
|
Neoplasms
|
Obesity
|
Occupational Diseases
|
Orofacial Cleft 10
|
Parkinsonian Disorders
|
Plaque, Atherosclerotic
|
Pneumonia
|
Recurrence
|
Skin Abnormalities
|
Skin Diseases
|
Drug Dependence
|
Sunburn
|
Uterine Cervical Neoplasms
|
Vitamin A Deficiency
|
Xeroderma Pigmentosum
|
Xeroderma Pigmentosum, Complementation Group B
|
Xeroderma Pigmentosum, Complementation Group C
|
Xeroderma Pigmentosum, Complementation Group D
|
Xeroderma Pigmentosum, Complementation Group E
|
Xeroderma Pigmentosum, Complementation Group F
|
Xfe Progeroid Syndrome
|
Androgenetic Alopecia
|
Amino Acid Metabolism, Inborn Errors
|
Anemia
|
Asthma
|
Atherosclerosis
|
Autism
|
Brain Injuries
|
Brain Ischemia
|
Breast Carcinoma
|
Carcinoma
|
Basal Cell Carcinoma
|
Carcinoma, Non-Small-Cell Lung
|
Squamous Cell Carcinoma
|