|
2071
|
|
|
Diacylglycerol kinase kappa |
- |
|
|
2072
|
|
|
Corticotropin releasing hormone |
CRF, CRH1 |
Alopecia, Alopecia, male pattern, Alzheimer disease, Androgenetic alopecia, Anhedonia, Anorexia, Anxiety disorder, Bipolar disorder, Clonic seizures, Cognitive disorder, Cryptogenic west syndrome, Cushing`s syndrome, Dysthymic disorder, Grand mal status epilepticus, Hypotonic seizures, Jackknife seizures, Jacksonian seizure, Melancholia, Mental depression, Mood disorder, Movement disorders, Neuroretinitis, Nocturnal epilepsy, Nonconvulsive status epilepticus, Petit mal status, Pituitary apoplexy, Pseudopelade, Psychomotor disorders, Retinitis, Salaam seizures, Schizophrenia, Seizure, Senile dementia, Spasmus nutans, Status epilepticus, Status marmoratus, Symptomatic west syndrome, West syndromeView all (23 more) |
|
2073
|
|
|
Dynein axonemal assembly factor 6 |
CILD36, CXorf41, NYSAR97, PIH1D3, TWISTER |
Asthenozoospermia, Asthma, Bronchiectasis, Congenital alveolar dysplasia, Ciliary dyskinesia, Ciliary dyskinesia, x-linked, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Bronchitis, Hearing loss, Hydrocephalus, Kartagener syndrome, Lung diseases, Nasal polyposis, Otitis media, Rhinitis, Scoliosis, Sinusitis, Situs inversusView all (5 more) |
|
2074
|
|
|
APC membrane recruitment protein 1 |
FAM123B, OSCS, WTX |
Aortic coarctation, Aortic valve sclerosis, Aphasia, Arachnodactyly, Atrial septal defect, Brachycephaly, Camptodactyly of fingers, Cataract, Congenital camptodactyly, Congenital clubfoot, Congenital epicanthus, Congenital malrotation of intestine, Congenital pectus excavatum, Developmental delay, Dwarfism, Dysmorphic features, Dysphasia, Facial paralysis, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Hydrocephalus, Laryngeal web, Macrocephaly, Mental retardation, Micrognathism, Microtia, Multiple congenital anomalies, Neck webbing, Nephroblastoma, Osteopathia striata, Osteopathia striata cranial sclerosis, Osteopetrosis, Partial agenesis of corpus callosum, Patent ductus arteriosus, Pierre-robin syndrome, Posteriorly rotated ear, Scoliosis, Specific learning disorder, Spina bifida occulta, Submucosal cleft palate, Tracheomalacia, Ventricular septal defect, Wilms tumorView all (29 more) |
|
2075
|
|
|
Corticotropin releasing hormone binding protein |
CRF-BP, CRFBP |
|
|
2076
|
|
|
Corticotropin releasing hormone receptor 1 |
CRF-R, CRF-R-1, CRF-R1, CRF1, CRFR-1, CRFR1, CRH-R-1, CRH-R1, CRHR, CRHR1L |
Alopecia, male pattern, Anhedonia, Anorexia, Anxiety disorder, Bipolar disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Dermatitis, Involutional depression, Involutional paraphrenia, Marfan syndrome, Mental depression, Mood disorder, Nonorganic psychosis, Osteoarthritis of hip, Parkinson disease, PsychosisView all (3 more) |
|
2077
|
|
|
Patched domain containing 1 |
AUTSX4, CXDELp22.11, DELXP22.11, SLC65C1 |
Attention deficit hyperactivity disorder, Autism, Autism spectrum disorder, Developmental delay, Facial paralysis, Macrocephaly, Meckel diverticulum, Mental retardation, Mental retardation, x-linked, Movement disorders, Neurosensory hearing impairment, Non-syndromic intellectual disability, x-linked, Obesity, Seizure, Syndactyly of the toes |
|
2078
|
|
|
Protein phosphatase 4 regulatory subunit 3C |
FLFL3P, PPP4R3CP, SMEK3P, smk1 |
|
|
2079
|
|
|
Corticotropin releasing hormone receptor 2 |
CRF-RB, CRF2, CRFR2, HM-CRF |
|
|
2080
|
|
|
Forkhead box R2 |
FOXN6 |
|
