991
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
992
|
|
|
Paired like homeobox 2A |
ARIX, CFEOM2, FEOM2, NCAM2, PMX2A |
Curated: Congenital fibrosis of extraocular muscles
Unreviewed: Cervical Cancer, Cervical Tumor, Cervix carcinoma, Epilepsy, Exotropia, Fibrosis Of Extraocular Muscles, Hypertension, Hypotropia, Mental retardation, Myopathy, Neoplasms, Neuroblastoma, Ptosis, Retinal detachment, Strabismus, Uterine neoplasm
|
993
|
|
|
Paired like homeobox 2B |
CCHS, NBLST2, NBPhox, PMX2B |
Curated: Haddad syndrome, Central hypoventilation syndrome, Congenital central hypoventilation syndrome, Crohn disease, Hirschsprung disease, Neuroblastoma, Schizophrenia
Unreviewed: Adrenal Gland Pheochromocytoma, alpha-Thalassemia Mental Retardation Syndrome, X-Linked, Apnea, Arnold-Chiari malformation, Arteriosclerosis, Atherosclerosis, Autonomic Central Nervous System Diseases, Autonomic nervous system disease, Bone marrow diseases, Brain neoplasms, Brain stem neoplasms, Cardiovascular Abnormalities, Cardiovascular disease, Central nervous system neoplasm, Chronobiology disorder, Colonic Aganglionosis, Congenital Central Hypoventilation, Congenital heart defect, Congenital Heart Disease, Congenital myopathy with fiber type disproportion, Coronary Heart Disease, Crohn Disease, Crohn`s Disease Of Large Bowel, Crohn`s Disease Of The Ileum, Developmental disability, Disruptive, impulse control, and conduct disorders, Diverticular disease, Diverticular Diseases, Diverticulitis, Dysautonomia, Dyscognitive seizures, Epilepsy, Episodic ataxia, Ganglioneuroblastoma, Ganglioneuroma, Gastroesophageal Reflux Disease, Gastrointestinal Diseases, Glioma, Hearing Loss, Hirschsprung Disease, Hirschsprung Disease Ganglioneuroblastoma, Hirschsprung Disease-Ganglioneuroblastoma Syndrome, Hypercapnia, Hyperoxaluria, Hypertension, Hypoxia, Ileocolitis, Impaired Cognition, Inflammatory Bowel Disease, Intestinal Pseudoobstruction, Lung Diseases, Lymphoblastic Leukemia, Malignant Neoplasm, Malocclusion, Medulloblastoma, Mental retardation, Miscarriage, Mouth Abnormalities, Mowat-Wilson Syndrome, Neoplasms, Nephroblastoma, Nervous System Neoplasms, Neural Crest Tumor, Neurodevelopmental Disorders, Ondine Syndrome, Paraganglioma, Parkinson disease, Pheochromocytoma, Pineoblastoma, Posteriorly Rotated Ear, Respiration Disorders, Respiratory Failure, Respiratory system infectious disease, Respiratory Tract Diseases, Retinoblastoma, Rhabdomyosarcoma, Sleep Apnea, Strabismus, Trisomy, Wilms tumor
|
994
|
|
|
PHOX2B antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
995
|
|
|
Phosphohistidine phosphatase 1 |
CGI-202, HEL-S-132P, HSPC141, PHP, PHP14 |
Curated: N/A
Unreviewed: Beckwith-Wiedemann Syndrome, Brachydactyly, Breast Cancer, Breast Carcinoma, Colorectal neoplasm, Congenital Hypothyroidism, Diabetes Mellitus, Dwarfism, Hypoparathyroidism, Liver Fibrosis, Lung Cancer, Lung carcinoma, Neoplasm of head, Neoplasms, Neurodegenerative Disorders, Obesity, Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism, Renal cell carcinoma, Turner Syndrome, Usher Syndrome
|
996
|
|
|
PHD and ring finger domains 1 |
PPP1R125, RNF221 |
Curated: Hirschsprung disease, Hypothyroidism, Systemic lupus erythematosus, Rheumatoid arthritis, Systemic sclerosis
Unreviewed: Ataxia telangiectasia, Breast Cancer, Breast Carcinoma, Kidney disease, Lung carcinoma, Lupus Erythematosus, Lupus Vulgaris, Malignant Neoplasm, Multiple Sclerosis, Neoplasms, Nonbacterial verrucal endocardiosis, Scleroderma, Sjogren syndrome
|
997
|
|
|
Putative homeodomain transcription factor 1 |
PHTF |
Curated: Ankylosing spondylitis, Anti-neutrophil antibody associated vasculitis, Asthma, Autoimmune disease, Autoimmune thyroid disease, Basal cell carcinoma, Celiac disease, Common variable immunodeficiency, Crohn disease, Diabetic ketoacidosis, Hyperthyroidism, Hypothyroidism, Inflammatory bowel disease, Juvenile idiopathic arthritis, Keratinocyte carcinoma, Multiple sclerosis, Myositis, Non-melanoma skin carcinoma, Oligoarticular juvenile idiopathic arthritis, Polyarticular juvenile idiopathic arthritis, Psoriasis, Rheumatoid arthritis, Skin cancer, Skin disease, Skin neoplasms, Systemic lupus erythematosus, Systemic sclerosis, Thyroid disease, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis, Vitiligo
Unreviewed: Breast neoplasm, Cardiomyopathy, Diabetes Mellitus, Diabetes mellitus, type 1, Duchenne muscular dystrophy, Juvenile arthritis, Pernicious anemia
|
998
|
|
|
Putative homeodomain transcription factor 2 |
- |
Curated: Atrial fibrillation, Cardioembolic stroke, Dental caries, Hypertension, Major depressive disorder, Obesity
Unreviewed: Leiomyoma, Lung carcinoma
|
999
|
|
|
Phytanoyl-CoA 2-hydroxylase |
LN1, LNAP1, PAHX, PHYH1, RD |
Curated: Refsum disease, Optic atrophy, Orofacial cleft, Peroxisomal disorder, Retinitis pigmentosa, phytanoyl-CoA hydroxylase deficiency
Unreviewed: Adrenoleukodystrophy, Cardiomyopathy, Cataract, Congestive Heart Failure, Crohn disease, Developmental regression, Disorder Of Eye, Drachtman Weinblatt Sitarz syndrome, Dysbiosis, Hearing Loss, Heart Block, Hemiplegia/hemiparesis, Hepatocellular carcinoma, Ichthyosis, Lupus Nephritis, Mental retardation, Microphthalmos, Miosis Disorder, Multiple Epiphyseal Dysplasia, Nail Diseases, Nail dysplasia, Nervous System Diseases, Nyctalopia, Nystagmus, Osteochondrodysplasia, Ptosis, Refsum Disease, Renal cell carcinoma, Renal Insufficiency, Retinal Diseases, Retinitis Pigmentosa, Rod-cone dystrophy, Sensorimotor neuropathy, Skeletal Dysplasia
|
1000
|
|
|
Phytanoyl-CoA dioxygenase domain containing 1 |
- |
Curated: N/A
Unreviewed: Alzheimer disease, Diabetic neuropathy, Lewy Body Disease, Parkinson disease
|