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Query OMIM entry list
189972
GTF2H1
GENERAL TRANSCRIPTION FACTOR IIH, POLYPEPTIDE 1
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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
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cockayne Syndrome
Skin Abnormalities
Ichthyosis
Xeroderma Pigmentosum
Genetic Diseases, Inborn
Dwarfism
Cockayne Syndrome
Heredodegenerative Disorders, Nervous System
Cockayne Syndrome
Skin Diseases, Genetic
Xeroderma Pigmentosum
Infant, Newborn, Diseases
Ichthyosis
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Ichthyosis
Photosensitivity Disorders
Xeroderma Pigmentosum
Pigmentation Disorders
Xeroderma Pigmentosum
Skin Abnormalities
Ichthyosis
Xeroderma Pigmentosum
Skin Diseases, Genetic
Xeroderma Pigmentosum
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Cockayne Syndrome
Xeroderma Pigmentosum
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
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