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181
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|
|
Gap junction protein beta 1 |
CMTX, CMTX1, CX32 |
Adenoma, Broca aphasia, Cerebellar ataxia, Cerebellar ataxia, x-linked, Charcot-marie-tooth disease, Charcot-marie-tooth disease, x-linked, Chromophobe carcinoma, Congenital pes cavus, Distal amyotrophy, Distal lower limb amyotrophy, Distal muscular atrophy, Distal upper limb amyotrophy, Dysarthria, Dysphagia, Language disorders, Liver neoplasms, Liver cancer, Liver carcinoma, Lung neoplasms, Lung cancer, Motor delay, Movement disorders, Nervous system diseases, Nystagmus, Papillary adenoma, Papillary renal carcinoma, Peroneal muscle atrophy, Renal carcinoma, Scoliosis, Sensorimotor neuropathy, Sensory neuropathy, Spinocerebellar degenerationView all (17 more) |
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182
|
|
|
Gap junction protein beta 2 |
BAPS, CX26, DFNA3, DFNA3A, DFNB1, DFNB1A, HID, KID, NSRD1, PPK |
Alopecia, Amniotic bands, Arthritis, Attention deficit hyperactivity disorder, Autism, Brachydactyly, Carcinoma, Cerebellar hypoplasia, Clinodactyly, Congenital omphalocele, Corneal erosion, Corneal neovascularization, Corneal ulcer, Cryptorchidism, Deafness, Deafness, digenic, Developmental delay, Drachtman weinblatt sitarz syndrome, Dwarfism, Dysmorphic features, Elbow flexion contracture, Erosion of cornea, Exfoliative dermatitis, Hearing loss, Hemiplegia/hemiparesis, Hidradenitis suppurativa, Hidrotic ectodermal dysplasia, Hirschsprung disease, Horseshoe kidney, Hyperkeratosis, Hypogonadotropic hypogonadism, Hypohidrosis, Hystrix-like ichthyosis with deafness, Ichthyosis, Ichthyosis follicularis atrichia photophobia syndrome, Impaired cognition, Keratitis, Keratitis ichthyosis and deafness syndrome, Keratoconjunctivitis sicca, Keratoderma hereditarium mutilans, Keratoderma with deafness, Kid syndrome, Knuckle pads, deafness and leukonychia syndrome, Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome, Leukoplakia, Macrostomia, Meleda disease, Mental retardation, Mutilating keratoderma, Nail diseases, Nail dysplasia, Nail dystrophy, Non-syndromic sensorineural deafness, Palmoplantar keratoderma with deafness, Palmoplantar keratoderma, Palmoplantar keratosis, Palmoplantar pustules, Porokeratotic eccrine ostial and dermal duct nevus, Pseudopelade, Psoriasis, Pulmonary arterial hypertension, Punctate keratitis, Sensorineural hearing loss, Senter syndrome, Skin cancer, Skin neoplasms, Skin carcinoma, Synophrys, Temporal hypotrichosis, Trichiasis, Urticaria, XerodermaView all (57 more) |
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183
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|
|
Gap junction protein beta 3 |
CX31, DFNA2, DFNA2B, EKV, EKVP1 |
Alopecia, Brachydactyly, Cataract, Deafness, Deafness, digenic, Dermatologic disorders, Diabetes mellitus, Dwarfism, Erythrokeratoderma, Erythrokeratodermia variabilis, Erythrokeratodermia variabilis et progressiva, Glaucoma, Hearing loss, Hyperkeratosis, epidermolytic, Mental retardation, Microcephaly, Nervous system diseases, Neuropathy with hearing impairment, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Patchy palmoplantar keratoderma, Skin neoplasmsView all (7 more) |
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184
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|
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Gap junction protein beta 5 |
CX31.1 |
|
|
185
|
|
|
Glycerol kinase |
GK1, GKD |
Deficiency of glycerol kinase, Developmental delay, Dwarfism, Frontal bossing, Glycerol kinase deficiency, Hypoglycemia, Ketosis, Mental retardation, Muscular dystrophy, Myocardial ischemia, Myopathy, Osteoporosis, Strabismus |
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186
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|
|
Galactosidase alpha |
GALA |
Achalasia, Anemia, Angiokeratoma, Anorexia, Anxiety disorder, Arthritis, Atrioventricular block, Bundle branch block, Cardiomyopathy, Cataract, Cerebral microangiopathy, Chronic obstructive pulmonary disease, Congestive heart failure, Conjunctival telangiectasis, Corneal dystrophy, Developmental regression, Diabetes insipidus, Dwarfism, Dysautonomia, Fabry disease, Fabry disease, cardiac variant, Hearing loss, Hyperkeratosis, Hyperlipidemia, Hypertension, Hypertrophic cardiomyopathy, Hypohidrosis, Impaired cognition, Ischemic stroke, Kidney disease, Kidney failure, Left ventricular hypertrophy, Lung diseases, Malabsorption syndrome, Mental depression, Moyamoya disease, Myocardial infarction, Nephritis, Nephrotic syndrome, Optic atrophy, Renal glomerular disease, Renal insufficiency, Stroke, Transient ischemic attack, Ventricular septal hypertrophyView all (30 more) |
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187
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|
|
Glypican 3 |
DGSX, GTR2-2, MXR7, OCI-5, SDYS, SGB, SGBS, SGBS1 |
Abnormal spinal segmentation, Accessory nipple, Agenesis of corpus callosum, Aniridia, Atrial septal defect, Bundle branch block, Camptodactyly of fingers, Cardiomyopathy, Congenital clubfoot, Congenital diaphragmatic hernia, Developmental dysplasia of the hip, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Congenital malrotation of intestine, Congenital omphalocele, Congenital pectus excavatum, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Double ureter, Hepatoblastoma, Hydrocephalus, Hydronephrosis, Hypertension, Hypoglycemia, Hypospadias, Liver neoplasms, Liver carcinoma, Lung neoplasms, Macrocephaly, Macroglossia, Macrostomia, Malocclusion, Meckel diverticulum, Mental retardation, Mesothelioma, Multicystic renal dysplasia, Nail diseases, Nail dysplasia, Neck webbing, Nephroblastoma, Neuroblastoma, Patent ductus arteriosus, Polydactyly, Polysplenia, Pulmonary stenosis, Renal cyst, Scoliosis, Simpson-golabi-behmel syndrome, Spade-like hand, Speech disorders, Syndactyly of fingers, Syndactyly of the toes, Talipes transversoplanus, Transposition of great vessels, Postaxial hand polydactyly, Ventricular septal defect, Wilms tumorView all (44 more) |
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188
|
|
|
Galactosidase beta 1 |
EBP, ELNR1, MPS4B |
Aortic valve sclerosis, Asthma, Beta-galactosidase deficiency, Bone disease, Cardiomyopathy, Cerebral atrophy, Cervical myelopathy, Chondrodystrophic myotonia, Congestive heart failure, Degenerative brain disorder, Dermatitis, Dwarfism, Dyschondroplasias, Eczema, Fabry disease, Frontal bossing, Galns deficiency, Gangliosidosis, Gangliosidosis, with cardiac involvement, Gm1 gangliosidosis, Hypertrichosis, Hypertrophic cardiomyopathy, Macrostomia, Malocclusion, Melnick-needles syndrome, Mental retardation, Mucopolysaccharidosis, Multiple epiphyseal dysplasia, Myoclonic seizures, Optic atrophy, Osteochondrodysplasia, Osteoporosis, Prostate cancer, Respiratory tract diseases, Schwartz-jampel syndrome, Scoliosis, Sea-blue histiocytosis, Spastic quadriplegia, Spondyloenchondrodysplasia, Spondyloepiphyseal dysplasia, Van buchem diseaseView all (26 more) |
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189
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|
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G protein-coupled receptor 78 |
- |
|
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190
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|
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- |
- |
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