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256540
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NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY
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Neoplasms
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Dysostoses
Bone Diseases, Metabolic
Mucolipidoses
Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Malabsorption Syndromes
Lactose Intolerance
Liver Diseases
Hepatomegaly
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Cerebellar Diseases
Cerebellar Ataxia
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Dementia
Epilepsy
Epilepsies, Myoclonic
Seizures
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Myoclonus
Neurobehavioral Manifestations
Intellectual Disability
Seizures
Sensation Disorders
Hearing Disorders
Eye Diseases
Eye Manifestations
Retinal Diseases
Male Urogenital Diseases
Urologic Diseases
Urination Disorders
Proteinuria
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Urination Disorders
Proteinuria
Pregnancy Complications
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Heart Valve Diseases
Aortic Valve Insufficiency
Mitral Valve Insufficiency
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Blood Platelet Disorders
Thrombocytopenia
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Lymphatic Diseases
Histiocytosis
Histiocytosis, Non-Langerhans-Cell
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Genetic Diseases, Inborn
Dwarfism
Genetic Diseases, X-Linked
Fabry Disease
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Carbohydrate Metabolism, Inborn Errors
Lactose Intolerance
Mucolipidoses
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 2
Lipid Metabolism Disorders
Lipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Malabsorption Syndromes
Lactose Intolerance
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Carbohydrate Metabolism, Inborn Errors
Lactose Intolerance
Mucolipidoses
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Endocrine System Diseases
Diabetes Mellitus
Diabetes Mellitus, Type 2
Dwarfism
Immune System Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Animal Diseases
Sheep Diseases
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Cardiomegaly
Hepatomegaly
Splenomegaly
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Ring Chromosomes
Translocation, Genetic
Disease
Syndrome
Growth Disorders
Signs and Symptoms
Edema
Hydrops Fetalis
Eye Manifestations
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Myoclonus
Neurobehavioral Manifestations
Intellectual Disability
Seizures
Sensation Disorders
Hearing Disorders
Skin Manifestations
Urological Manifestations
Proteinuria
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