MeSH Treeview
Query OMIM entry list
300017
FLNA
FILAMIN A
→
High-scoring List
Neoplasms
Hamartoma
Tuberous Sclerosis
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Nevi and Melanomas
Melanoma
Neoplasms by Site
Nervous System Neoplasms
Central Nervous System Neoplasms
Brain Neoplasms
Cerebral Ventricle Neoplasms
Urogenital Neoplasms
Genital Neoplasms, Male
Prostatic Neoplasms
Neoplasms, Multiple Primary
Tuberous Sclerosis
Neoplastic Syndromes, Hereditary
Tuberous Sclerosis
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Synostosis
Syndactyly
Osteochondrodysplasias
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Limb Deformities, Congenital
Syndactyly
Synostosis
Syndactyly
Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Intestinal Obstruction
Ileus
Intestinal Pseudo-Obstruction
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Mouth Diseases
Mouth Abnormalities
Cleft Palate
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Mouth Abnormalities
Cleft Palate
Respiratory Tract Diseases
Lung Diseases
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Hearing Loss, Bilateral
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Neoplasms
Cerebral Ventricle Neoplasms
Cerebrovascular Disorders
Epilepsy
Epilepsies, Partial
Epilepsy, Complex Partial
Epilepsy, Generalized
Spasms, Infantile
Seizures
Hydrocephalus
Intracranial Hypertension
Hydrocephalus
Nervous System Malformations
Malformations of Cortical Development
Tuberous Sclerosis
Nervous System Neoplasms
Central Nervous System Neoplasms
Brain Neoplasms
Cerebral Ventricle Neoplasms
Neurocutaneous Syndromes
Tuberous Sclerosis
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Tuberous Sclerosis
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Pupil Disorders
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Bilateral
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Eye Diseases
Eye Abnormalities
Pupil Disorders
Male Urogenital Diseases
Genital Diseases, Male
Genital Neoplasms, Male
Prostatic Neoplasms
Prostatic Diseases
Prostatic Neoplasms
Urogenital Neoplasms
Genital Neoplasms, Male
Prostatic Neoplasms
Urologic Diseases
Kidney Diseases
Nephrosis
Nephrosis, Lipoid
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephrosis
Nephrosis, Lipoid
Pregnancy Complications
Abortion, Spontaneous
Embryo Loss
Fetal Death
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Diseases
Heart Defects, Congenital
Heart Failure
Heart Valve Diseases
Vascular Diseases
Cerebrovascular Disorders
Hemostatic Disorders
Ehlers-Danlos Syndrome
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemorrhagic Disorders
Hemostatic Disorders
Ehlers-Danlos Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cardiovascular Abnormalities
Heart Defects, Congenital
Eye Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Limb Deformities, Congenital
Syndactyly
Synostosis
Syndactyly
Nervous System Malformations
Malformations of Cortical Development
Tuberous Sclerosis
Skin Abnormalities
Ehlers-Danlos Syndrome
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Mouth Abnormalities
Cleft Palate
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Heredodegenerative Disorders, Nervous System
Tuberous Sclerosis
Muscular Dystrophies
Neoplastic Syndromes, Hereditary
Tuberous Sclerosis
Skin Diseases, Genetic
Ehlers-Danlos Syndrome
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Ehlers-Danlos Syndrome
Skin Diseases
Skin Abnormalities
Ehlers-Danlos Syndrome
Skin Diseases, Genetic
Ehlers-Danlos Syndrome
Animal Diseases
Disease Models, Animal
Muscular Dystrophy, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Choristoma
Pathologic Processes
Chromosome Aberrations
Chromosome Breakage
Chromosome Inversion
Sex Chromosome Aberrations
Translocation, Genetic
Death
Embryo Loss
Fetal Death
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Growth Disorders
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Pupil Disorders
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Bilateral
Signs and Symptoms, Digestive
Constipation
Database Center for Life Science