190381
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Transient receptor potential cation channel subfamily V member 3 |
FNEPPK2, OLMS, OLMS1, VRL3 |
Curated: Congenital palmoplantar and perioral keratoderma of olmsted, Gestational diabetes, Hyperplasia, Migraine, Oguchi disease, Olmsted syndrome, Schizophrenia
Unreviewed: Alopecia, Anhidrosis, Atopic dermatitis, Atrial fibrillation, Behcet disease, Cardioembolic Stroke, Cholesteatoma, Congenital hyperinsulinism, Dermatitis, Dermatologic Disorders, Diabetes mellitus, Diabetes mellitus, type 2, Diabetic neuropathy, Eczema, Epidermolytic hyperkeratosis, Erythromelalgia, Gastrointestinal inflammation, Growth disorder, Hearing Loss, Hyperhidrosis Palmaris Et Plantaris, Hyperkeratosis, Hypodontia, Hypotrichosis, Irritable bowel syndrome, Isolated Focal Non-Epidermolytic Palmoplantar Keratoderma, Lung Cancer, Lung carcinoma, Lung Neoplasms, Melanoma, Meningioma, Migraine with Aura, Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Nail Diseases, Nail dysplasia, Nail dystrophy, Nasal polyp, Nasal polyposis, Nonepidermolytic palmoplantar keratoderma, Olmsted Syndrome, Pachyonychia congenita, Palmoplantar keratoderma, Parakeratosis, Pruritus, Pterygium, Pulmonary arterial hypertension, Renal cell carcinoma, Rosacea, Sinusitis, Skin disease, Skin Lesion, Skin neoplasm, Skin Neoplasms, Squamous cell carcinoma, Subungual hyperkeratosis, Ulcerative colitis
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190382
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Transient receptor potential cation channel subfamily V member 4 |
BCYM3, CMT2C, HMSN2C, OTRPC4, SMAL, SPSMA, SSQTL1, TRP12, VRL2, VROAC |
Curated: Alzheimer disease, Osteonecrosis of the femoral head, Auditory neuropathy, Brachyolmia, Charcot-marie-tooth disease, Congenital benign spinal muscular atrophy, Distal hereditary motor neuropathy, Avascular necrosis of bone, Avascular necrosis of femoral head, Bone disease, Brachyrachia, Obstructive airway disease, Congenital cartilage disorder, Congenital clubfoot, Connective tissue disease, Dejerine-sottas disease, Desbuquois syndrome, Digital arthropathy-brachydactyly, familial, Distal spinal muscular atrophy, Glioma, Gout, Hereditary motor and sensory neuropathies, Motor neuron disease, Hyperalgesia, Hypertrophic neuropathy, Neuromuscular disease, Osteoarthritis, Osteochondrodysplasias, Osteonecrosis of medial femoral condyle, Parastremmatic dwarfism, Peroneal muscle atrophy, Chronic obstructive pulmonary disease, Roussy-levy syndrome, Scapuloperoneal spinal muscular atrophy, Schizophrenia, Skeletal dysplasia, Spinal muscular atrophy, Spondyloepimetaphyseal dysplasia, Spondyloepiphyseal dysplasia, Spondylometaphyseal dysplasia, Urination disorders, TRPV4-related bone disorder
Unreviewed: Abducens palsy, Acoustic Neuroma, Acquired Kyphoscoliosis, Agenesis Of Corpus Callosum, Akinesia, Aortic Valve Sclerosis, Aplasia Of Muscle, Arteriosclerosis, Arthritis, Arthrogryposis, Arthrogryposis multiplex congenita, Arthropathy, Aseptic necrosis, Asthma, Astrocytoma, Atherosclerosis, Atrial fibrillation, Avascular Necrosis Of Femoral Head, Avascular Necrosis Of The Capital Femoral Epiphysis, Bone Disease, Brachydactyly, Brain edema, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bulbospinal Neuronopathy, Camptodactyly of fingers, Carcinogenesis, Cardiomyopathy, Cardiovascular Diseases, Cartilage disease, Cataract, Central Nervous System Demyelination, Cerebral Infarction, Cerebral Ischemia, Charcot-Marie-Tooth Disease, Cholesteatoma, Chondrodystrophic myotonia, Chronic Obstructive Pulmonary Disease, Clinodactyly, Colitis, Colon Carcinoma, Colonic neoplasm, Colonic Neoplasms, Colorectal neoplasm, Congenital Clubfoot, Congenital kyphoscoliosis, CONGENITAL NONPROGRESSIVE SPINAL MUSCULAR ATROPHY, Congenital Pectus Carinatum, Congestive Heart Failure, Craniosynostosis, Cystic Fibrosis, Cystitis, Dementia, Derealization, Dermatitis, Dermatologic Disorders, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Neuralgia, Diabetic neuropathy, Diabetic Retinopathy, Digital Arthropathy-Brachydactyly, Distal amyotrophy, Distal hereditary motor neuronopathy, Distal Muscular Atrophy, Distal Spinal Muscular Atrophy, Distal spinal muscular atrophy, congenital nonprogressive, Dwarfism, Dysautonomia, Dyschondroplasias, Dysmorphic Features, Dysphasia, Edema, Elbow flexion contracture, Endometriosis, Epilepsy, Epiphyseal dysplasia, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Facial paralysis, Fatty Liver, Femur Head Necrosis, Functional Gastrointestinal Disorders, Gastroesophageal Reflux Disease, Gastrointestinal inflammation, Gaucher disease, Glaucoma, Growth disorder, Hearing Loss, Hereditary motor and sensory neuropathy, Hereditary sensory and motor neuropathy, Hip Contracture, Hydrocephalus, Hypercalcemia, Hyperglycemia, Hyperopia, Hypersomnia, Hypertension, Hypertrophy, Hypophosphatasia, Impaired Cognition, Inflammatory Bowel Disease, Intervertebral Disc Degeneration, Intervertebral disc disease, Irritable Bowel Syndrome, Ischemic Stroke, Kallmann syndrome, Kidney Disease, Kidney Failure, Legg-Calve-Perthes Disease, Liver carcinoma, Liver Fibrosis, Lung Diseases, Lung neoplasms, Major depressive disorder, Malignant Neoplasm, Melanoma, Melnick-Needles Syndrome, Meniere Disease, Meningioma, Mental retardation, Metabolic Diseases, Metabolic syndrome, Metatropic Dwarfism, Metatropic Dysplasia, Micromelia, Motor delay, Motor nerve neuritis, Mucopolysaccharidosis, Multiple Congenital Anomalies, Multiple Epiphyseal Dysplasia, Muscular Atrophy, Myelopathic Muscular Atrophy, Nasal polyposis, Neoplasms, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Neuromuscular Diseases, Neuropathy, Non-Alcoholic Fatty Liver Disease, Obesity, Ocular Hypertension, Oculomotor nerve palsy, Oculopharyngeal Spinal Muscular Atrophy, Osteoarthritis Of Hip, Osteoarthritis Of The Hand, Osteoarthrosis Deformans, Osteochondrodysplasia, Osteogenesis imperfecta, Osteonecrosis, Osteopenia, Osteoporosis, Parastremmatic Dwarfism, Partial Paralysis Vocal Cords, Periodontal Diseases, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Polycystic kidney disease, Polyneuropathy, Progressive Muscular Atrophy, Progressive Proximal Myelopathic Muscular Atrophy, Pterygium, Pulmonary arterial hypertension, Pulmonary Fibrosis, Pulmonary Hypertension, Renal cell carcinoma, Renal fibrosis, Renal Insufficiency, Respiration Disorders, Respiratory Failure, Respiratory system infectious disease, Respiratory Tract Diseases, Retinal Detachment, Retinal Diseases, Rheumatoid arthritis, Rosacea, Roussy-Levy Syndrome, Schwartz-Jampel Syndrome, Scleroderma, Scoliosis, Sensory neuropathy, Septicemia, Short-Trunk Short Stature, Sinusitis, Skeletal Dysplasia, Skin Carcinoma, Skin neoplasm, Sleep Apnea, Small cell lung carcinoma, Spinal cord compression, Spinal Muscular Atrophy, Spinocerebellar Ataxia, Spondyloenchondrodysplasia, Spondyloepiphyseal dysplasia congenita, Spondylometaphyseal Dysplasia, Squamous cell carcinoma, Status Epilepticus, Stomach Carcinoma, Stomach Neoplasms, Stroke, Strudwick Syndrome, Thrombocytosis, Trigeminal neuralgia, Ulcerative colitis, Urination Disorders, Van Buchem Disease, Vocal Cord Paralysis, Vulval varices
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190383
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Transient receptor potential cation channel subfamily V member 5 |
CAT2, ECAC1, OTRPC3 |
Curated: Bladder calculus, Hypercalciuria, Nephrolithiasis, Neurotic disorder, Diabetes mellitus type 2, Urolithiasis
Unreviewed: Arteriosclerosis, Arthritis, Atherosclerosis, Atrial fibrillation, B-Cell Lymphoma, Cataract, Cystic Fibrosis, Diabetes, Diabetes Mellitus, Gitelman Syndrome, Hypercalcemia, Hypertension, Hypocalciuric Hypercalcemia, Kidney Disease, Kidney stone, Leukemia, Lung carcinoma, Malignant Neoplasm, Metabolic syndrome, Myeloid leukemia, Neoplasms, Nephrocalcinosis, Proteinuria, Pseudohypoaldosteronism, Renal Carcinoma, Renal cell carcinoma, Septicemia, Ulcerative colitis
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190384
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Transient receptor potential cation channel subfamily V member 6 |
ABP/ZF, CAT1, CATL, ECAC2, HRPTTN, HSA277909, LP6728, ZFAB |
Curated: Hereditary chronic pancreatitis, Bladder calculus, Desbuquois syndrome, Hyperparathyroidism, Intestinal hypomagnesemia, Mastocytosis, Nephrolithiasis, Neurotic disorder, Pancreatitis, Polycystic ovary syndrome, Urolithiasis
Unreviewed: 5p partial monosomy syndrome, Adenocarcinoma, Arthritis, Atrial fibrillation, Benign Prostatic Hyperplasia, Bicuspid aortic valve, Bipolar Disorder, Breast Adenocarcinoma, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Cholesteatoma, Colon Carcinoma, Colonic neoplasm, Colonic Neoplasms, Colorectal Cancer, Congenital glucose-galactose malabsorption, Congestive Heart Failure, Cystic Fibrosis, Dermatologic Disorders, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Gastric Cancer, Hepatocellular carcinoma, Hereditary breast and ovarian cancer syndrome, Hypercalcemia, Hypertension, Hypocholesterolemia, Idiopathic pulmonary fibrosis, Leukemia, Liver carcinoma, Lung carcinoma, Lymphoma, Malignant Neoplasm, Mammary Neoplasms, Mental retardation, Metabolic syndrome, Metastatic Prostate Carcinoma, Microcephaly, Motor delay, Myeloid leukemia, Neoplasms, Nephrocalcinosis, Osteopenia, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Parathyroid Adenoma, Parkinson disease, Polycystic Ovary Syndrome, Prostate adenocarcinoma, Prostate cancer, Prostatic disease, Prostatic neoplasm, Prostatic Neoplasms, Renal cell carcinoma, Sarcoidosis, Sclerocystic Ovaries, Stomach Carcinoma, Stomach Neoplasms, Trichohepatoenteric Syndrome, Ulcerative colitis, Williams Syndrome
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