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610651
XPB
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Neoplasms, Glandular and Epithelial
Carcinoma
Carcinoma, Basal Cell
Carcinoma, Squamous Cell
Neoplasms, Basal Cell
Carcinoma, Basal Cell
Neoplasms, Squamous Cell
Carcinoma, Squamous Cell
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Nevi and Melanomas
Melanoma
Neoplasms by Site
Eye Neoplasms
Skin Neoplasms
Precancerous Conditions
Xeroderma Pigmentosum
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Cockayne Syndrome
Nervous System Diseases
Demyelinating Diseases
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Cockayne Syndrome
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Reflex, Abnormal
Eye Diseases
Eye Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cockayne Syndrome
Skin Abnormalities
Xeroderma Pigmentosum
Genetic Diseases, Inborn
Dwarfism
Cockayne Syndrome
Heredodegenerative Disorders, Nervous System
Cockayne Syndrome
Skin Diseases, Genetic
Xeroderma Pigmentosum
Skin and Connective Tissue Diseases
Skin Diseases
Hair Diseases
Photosensitivity Disorders
Xeroderma Pigmentosum
Pigmentation Disorders
Xeroderma Pigmentosum
Skin Abnormalities
Xeroderma Pigmentosum
Skin Diseases, Genetic
Xeroderma Pigmentosum
Skin Neoplasms
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Cockayne Syndrome
Xeroderma Pigmentosum
Endocrine System Diseases
Dwarfism
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Reflex, Abnormal
Skin Manifestations
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