281
|
|
|
KIAA0232 |
- |
Curated: Alzheimer disease, Language development disorders
Unreviewed: Esophageal squamous cell carcinoma
|
282
|
|
|
KIAA0319 |
DYLX2, DYX2, NMIG |
Curated: Colorectal cancer, Coronary artery disease, Major depressive disorder, Schizophrenia, Ulcerative colitis
Unreviewed: Apraxia, Atrophy, Attention deficit hyperactivity disorder, Autism Spectrum Disorder, Ciliary dyskinesia, Coronary Heart Disease, Development Disorder, Developmental dyslexia, Dyslexia, Episodic Kinesigenic Dyskinesia, Frontotemporal dementia, Glioblastoma, Glioma, Language development disorders, Language Disorders, Learning disorders, Lissencephaly, Lymphoma, Malformation of cortical development, Nervous System Disorder, Parkinson disease, Polycystic kidney disease, Wernicke Encephalopathy
|
283
|
|
|
KIAA0319 like |
AAVR, AAVRL |
Curated: Insomnia, Crest syndrome, Systemic lupus erythematosus, Systemic sclerosis, Diabetes mellitus type 1, Diabetes mellitus type 2
Unreviewed: Autoimmune Diseases, CREST Syndrome, Developmental dyslexia, Dyslexia, Dysphagia, Episodic Kinesigenic Dyskinesia, Gastroesophageal Reflux Disease, Learning Disorders, Limited Systemic Sclerosis, Lupus Erythematosus, Malformation of cortical development, Periventricular Nodular Heterotopia, Polycystic kidney disease, Pulmonary arterial hypertension, Pulmonary Fibrosis, Scleroderma
|
284
|
|
|
KIAA0408 |
- |
Curated: Astrocytoma, Diverticular disease, Metabolic syndrome, Diabetes mellitus type 2
Unreviewed: N/A
|
285
|
|
|
KIAA0513 |
- |
Curated: Amyotrophic lateral sclerosis, Atrophic macular degeneration, Scoliosis
Unreviewed: Alzheimer disease, Amyotrophic Lateral Sclerosis, Leukemia, Malignant Neoplasm, Neoplasms, Pancreatic neoplasm, Schizophrenia
|
286
|
|
|
KIAA0586 |
JBTS23, SRTD14, Talpid3 |
Curated: Jeune syndrome, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Congenital brain malformation, Congenital hypoplasia of part of brain, Craniofacial abnormalities, Desbuquois syndrome, Aplasia of the vermis, Hydranencephaly, Intellectual developmental disorder, Joubert syndrome, Jeune thoracic dystrophy, Lissencephaly, Macrogyria, Meckel-gruber syndrome, Microgyria, Neurodevelopmental disorder, Polydactyly, Rod-cone dystrophy, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia
Unreviewed: Absence Of Septum Pellucidum, Accessory Nipple, Anencephaly, Apraxia, Asphyxiating thoracic dystrophy, Atrial Septal Defect, Brachydactyly, Cerebellar Ataxia, Cerebellar diseases, Cerebellar Hypoplasia, Cerebellar vermis agenesis, Cholestasis, Ciliopathies, Ciliopathy, Colorectal neoplasm, Colpocephaly, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital diaphragmatic hernia, Congenital Epicanthus, Congenital Meningocele, Dandy-Walker Syndrome, Development Disorder, Developmental Delay, Dextrocardia, Diastrophic Dysplasia, Duane Retraction Syndrome, Frontal bossing, Fundus Coloboma, Gastroesophageal Reflux Disease, Hereditary Hemochromatosis, Hirschsprung Disease, Hydrocephalus, Hydrolethalus syndrome, Hypospadias, Jeune Thoracic Dystrophy, Joubert Syndrome, Joubert Syndrome With Jeune Asphyxiating Thoracic Dystrophy, Keratosis Follicularis, Lung Diseases, Majewski Syndrome, Meckel-Gruber Syndrome, Mental retardation, Micrognathism, Micromelia, MOHR-TRANEBJAERG SYNDROME, Myopia, Nystagmus, Occipital Encephalocele, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Oral cleft, Orofaciodigital syndrome, Penis Agenesis, Pericardial effusion, Polycystic kidney disease, Polydactyly Of Toes, Polymicrogyria, Ptosis, Pulmonary hypoplasia, Radial Polydactyly, Renal dysplasia, Renal Insufficiency, Retinal coloboma, Retinal Dystrophy, Scoliosis, Short Rib-Polydactyly Syndrome, Short-Rib Thoracic Dysplasia With Or Without Polydactyly, Situs Inversus, Strabismus, Stress urinary incontinence, Thoracic hypoplasia
|
287
|
|
|
KIAA0753 |
JBTS38, MNR, OFIP, SRTD21 |
Curated: Jeune syndrome, Congenital brain malformation, Congenital hypoplasia of part of brain, Desbuquois syndrome, Aplasia of the vermis, Hydranencephaly, Joubert syndrome, Jeune thoracic dystrophy, Lissencephaly, Lung cancer, Macrogyria, Microgyria, Orofaciodigital syndrome, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia
Unreviewed: Agenesis Of Corpus Callosum, Ataxia Telangiectasia, Brachydactyly, Cerebellar hypoplasia, Cerebellar vermis agenesis, Ciliopathies, Ciliopathy, Clinodactyly, Colorectal neoplasm, Congenital Epicanthus, Congenital heart defects, Cryptorchidism, Developmental Delay, Dwarfism, Esotropia, Frontal bossing, Hearing Loss, High palate, Hydronephrosis, Hypothalamic Hamartomas, Isolated Somatotropin Deficiency, Jeune Thoracic Dystrophy, Malformation of cortical development, Mental retardation, Micrognathism, Neoplasms, Nystagmus, Osteochondrodysplasia, Osteofibrous Dysplasia, Periventricular nodular heterotopia, Polydactyly, Polydactyly Of Toes, Radial Polydactyly, Renal agenesis, Skeletal Dysplasia, Somatotropin Deficiency, Syndactyly, Thoracic hypoplasia
|
288
|
|
|
KIAA0825 |
C5orf36, PAPA10 |
Curated: Dementia, Diabetic retinopathy, Gallbladder neoplasms, Hemorrhoid, Polydactyly, Postaxial polydactyly
Unreviewed: Diabetes mellitus, type 2, Diabetic Retinopathy, Foot Polydactyly, Hearing loss, Malignant Neoplasm
|
289
|
|
|
KIAA00895L pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
290
|
|
|
KIAA0930 |
C22orf9, LSC3 |
Curated: Melanoma, Neurodevelopmental disorder, Osteoarthritis, Psoriatic arthritis, Schizophrenia, Skin cancer, Skin neoplasms
Unreviewed: Leukemia, Lung neoplasms
|