MeSH Treeview
Query OMIM entry list
278780
XPG
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G
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Neoplasms
Neoplasms by Site
Skin Neoplasms
Precancerous Conditions
Xeroderma Pigmentosum
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Cockayne Syndrome
Nervous System Diseases
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Cockayne Syndrome
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cockayne Syndrome
Skin Abnormalities
Xeroderma Pigmentosum
Fetal Diseases
Genetic Diseases, Inborn
Dwarfism
Cockayne Syndrome
Heredodegenerative Disorders, Nervous System
Cockayne Syndrome
Skin Diseases, Genetic
Xeroderma Pigmentosum
Skin and Connective Tissue Diseases
Skin 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
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
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