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605799
AMN
AMNIONLESS, MOUSE, HOMOLOG OF
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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
Male Urogenital Diseases
Urologic Diseases
Urination Disorders
Proteinuria
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Urination Disorders
Proteinuria
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Macrocytic
Anemia, Megaloblastic
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
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Cockayne Syndrome
Xeroderma Pigmentosum
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin B Deficiency
Vitamin B 12 Deficiency
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Urological Manifestations
Proteinuria
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