MeSH Treeview
Query gene list
889
KRIT1
KRIT1, ankyrin repeat containing
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Connective and Soft Tissue
Neoplasms, Connective Tissue
Myxoma
Neoplasms, Muscle Tissue
Leiomyoma
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neuroendocrine Tumors
Neurilemmoma
Neuroma, Acoustic
Neoplasms, Nerve Tissue
Nerve Sheath Neoplasms
Neuroma
Neurilemmoma
Neuroma, Acoustic
Neuroectodermal Tumors
Neuroendocrine Tumors
Neurilemmoma
Neuroma, Acoustic
Neoplasms, Vascular Tissue
Angiokeratoma
Hemangioma
Hemangioma, Cavernous
Hemangioma, Cavernous, Central Nervous System
Nevi and Melanomas
Nevus
Neoplasms by Site
Bone Neoplasms
Spinal Neoplasms
Eye Neoplasms
Retinal Neoplasms
Nervous System Neoplasms
Central Nervous System Neoplasms
Brain Neoplasms
Spinal Cord Neoplasms
Peripheral Nervous System Neoplasms
Cranial Nerve Neoplasms
Neuroma, Acoustic
Skin Neoplasms
Thoracic Neoplasms
Heart Neoplasms
Neoplasms, Multiple Primary
Neoplastic Processes
Cell Transformation, Neoplastic
Neoplastic Syndromes, Hereditary
Musculoskeletal Diseases
Bone Diseases
Bone Neoplasms
Spinal Neoplasms
Spinal Diseases
Spinal Neoplasms
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Retrocochlear Diseases
Vestibulocochlear Nerve Diseases
Neuroma, Acoustic
Otorhinolaryngologic Neoplasms
Neuroma, Acoustic
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Neoplasms
Cerebellar Diseases
Cerebrovascular Disorders
Carotid Artery Diseases
Moyamoya Disease
Intracranial Arterial Diseases
Cerebral Arterial Diseases
Moyamoya Disease
Intracranial Arteriovenous Malformations
Intracranial Hemorrhages
Cerebral Hemorrhage
Stroke
Epilepsy
Seizures
Spinal Cord Diseases
Amyotrophic Lateral Sclerosis
Spinal Cord Neoplasms
Cranial Nerve Diseases
Cranial Nerve Neoplasms
Neuroma, Acoustic
Vestibulocochlear Nerve Diseases
Neuroma, Acoustic
Nervous System Malformations
Central Nervous System Vascular Malformations
Hemangioma, Cavernous, Central Nervous System
Intracranial Arteriovenous Malformations
Nervous System Neoplasms
Central Nervous System Neoplasms
Brain Neoplasms
Spinal Cord Neoplasms
Neurodegenerative Diseases
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Prader-Willi Syndrome
Williams Syndrome
Pain
Paralysis
Paresis
Paraparesis
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Neuromuscular Diseases
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Eye Diseases
Eye Neoplasms
Retinal Neoplasms
Retinal Diseases
Retinal Neoplasms
Cardiovascular Diseases
Cardiovascular Abnormalities
Vascular Malformations
Arteriovenous Malformations
Intracranial Arteriovenous Malformations
Central Nervous System Vascular Malformations
Hemangioma, Cavernous, Central Nervous System
Intracranial Arteriovenous Malformations
Heart Diseases
Heart Neoplasms
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Supravalvular
Williams Syndrome
Vascular Diseases
Arterial Occlusive Diseases
Moyamoya Disease
Arteriovenous Malformations
Intracranial Arteriovenous Malformations
Cerebrovascular Disorders
Carotid Artery Diseases
Moyamoya Disease
Intracranial Arterial Diseases
Cerebral Arterial Diseases
Moyamoya Disease
Intracranial Arteriovenous Malformations
Intracranial Hemorrhages
Cerebral Hemorrhage
Stroke
Embolism and Thrombosis
Thrombosis
Hemostatic Disorders
Hemangioma, Cavernous
Hemangioma, Cavernous, Central Nervous System
Telangiectasia, Hereditary Hemorrhagic
Telangiectasis
Telangiectasia, Hereditary Hemorrhagic
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemorrhagic Disorders
Hemostatic Disorders
Hemangioma, Cavernous
Hemangioma, Cavernous, Central Nervous System
Telangiectasia, Hereditary Hemorrhagic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Prader-Willi Syndrome
Cardiovascular Abnormalities
Vascular Malformations
Arteriovenous Malformations
Intracranial Arteriovenous Malformations
Central Nervous System Vascular Malformations
Intracranial Arteriovenous Malformations
Telangiectasia, Hereditary Hemorrhagic
Chromosome Disorders
Prader-Willi Syndrome
Williams Syndrome
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Nervous System Malformations
Central Nervous System Vascular Malformations
Hemangioma, Cavernous, Central Nervous System
Intracranial Arteriovenous Malformations
Skin Abnormalities
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Genetic Diseases, Inborn
Chromosome Disorders
Prader-Willi Syndrome
Williams Syndrome
Genetic Diseases, X-Linked
Muscular Dystrophy, Duchenne
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Neoplastic Syndromes, Hereditary
Skin Diseases, Genetic
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Infant, Newborn, Diseases
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Pigmentation Disorders
Cafe-au-Lait Spots
Skin Abnormalities
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin Diseases, Genetic
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin Neoplasms
Nutritional and Metabolic Diseases
Metabolic Diseases
Proteostasis Deficiencies
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Chromosomal Instability
Chromosome Fragility
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Hemorrhage
Intracranial Hemorrhages
Cerebral Hemorrhage
Metaplasia
Neovascularization, Pathologic
Neoplastic Processes
Cell Transformation, Neoplastic
Signs and Symptoms
Neurologic Manifestations
Pain
Paralysis
Paresis
Paraparesis
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Pain
Skin Manifestations
Cafe-au-Lait Spots
Database Center for Life Science