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231550
AAA
ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Digestive System Diseases
Gastrointestinal Diseases
Esophageal Diseases
Deglutition Disorders
Esophageal Motility Disorders
Esophageal Achalasia
Stomach Diseases
Respiratory Tract Diseases
Lung Diseases
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Autonomic Nervous System Diseases
Primary Dysautonomias
Dysautonomia, Familial
Central Nervous System Diseases
Brain Diseases
Dementia
Epilepsy
Seizures
Spinal Cord Diseases
Demyelinating Diseases
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Malformations of Cortical Development
Microcephaly
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Seizures
Sensation Disorders
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Eye Diseases
Conjunctival Diseases
Xerophthalmia
Lacrimal Apparatus Diseases
Dry Eye Syndromes
Xerophthalmia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Malformations of Cortical Development
Microcephaly
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Vitiligo
Nutritional and Metabolic Diseases
Metabolic Diseases
Glucose Metabolism Disorders
Hypoglycemia
Endocrine System Diseases
Adrenal Gland Diseases
Adrenal Insufficiency
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Seizures
Sensation Disorders
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