|
211
|
|
|
KH-type splicing regulatory protein pseudogene 1 |
- |
|
|
212
|
|
|
Karyopherin subunit alpha 7 |
IPOA8, OZEMA17 |
|
|
213
|
|
|
KIT ligand |
DCUA, DFNA69, FPH2, FPHH, KL-1, Kitl, MGF, SCF, SF, SHEP7, SLF, WS2F |
Anaplastic carcinoma, Anomalous pulmonary artery, Neoplasm, Carcinoma, Deafness, Embryonal neoplasm, Tumor, Hearing loss, Hirschsprung disease, Hyperkeratosis, Hyperpigmentation, Malignant neoplasm of testis, Malignant testicular germ cell tumor, Melanosis, Multicystic renal dysplasia, Multiple lentigines, Myocardial ischemia, Nasal polyposis, Nasopharyngeal carcinoma, Non-seminomatous tumor of testis, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Progressive hyper and hypopigmentation, Progressive hyperpigmentation, Ptosis, Tumor of rete testis, Testicular neoplasms, Testicular germ cell tumor, Waardenburg syndromeView all (14 more) |
|
214
|
|
|
Lysine methyltransferase 2A |
ALL-1, ALL1, CXXC7, GAS7, HRX, HTRX, HTRX1, MLL, MLL1, MLL1A, TRX1, WDSTS |
Adenocarcinoma, Ankyloglossia, Anxiety disorder, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Urinary bladder cancer, Bladder neoplasm, Blepharophimosis, Bowel incontinence, Brachycephaly, Burkitt`s lymphoma, Camptodactyly of fingers, Carcinoma, Cataract, Cerebral cortical atrophy, Cervical spine instability, Choanal atresia, Congenital diaphragmatic hernia, Congenital epicanthus, Congenital hypoplasia of penis, Congenital malrotation of intestine, Congenital pectus excavatum, Cornelia de lange syndrome, Cryptorchidism, Cutis marmorata, Developmental delay, Dolichocephaly, Drusen, Dwarfism, Dysmorphic features, Dysphagia, Dyssomnia, Elbow hypertrichosis, Erythroleukemia, Frontal bossing, Gastric cancer, Gastroesophageal reflux disease, Glaucoma, Growth deficiency and mental retardation with facial dysmorphism, Hearing loss, High palate, Hypertrichosis, Hypoplasia of corpus callosum, Hypoplasia of nipple, Hypospadias, Mental retardation, Intestinal volvulus, Isolated somatotropin deficiency, Kabuki syndrome, Klippel feil syndrome, Laryngomalacia, Leukemia, Lymphoblastic leukemia, Liver carcinoma, Lung carcinoma, Lymphoid leukemia, Macrotia, Mental depression, Microcephaly, Microcornea, Micrognathism, Micromelia, Microphthalmos, Microtia, Mixed phenotype leukemia, Monocytic leukemia, Movement disorders, Multicystic renal dysplasia, Multiple congenital anomalies, Myeloid leukemia, Myeloid leukemia with 11q23 abnormalities, Myeloid leukemia with t(9;11)(p22;q23), Myeloid leukemia, 11q23 abnormalities, Myelomonocytic leukemia, Myopia, Neck webbing, Nervous system diseases, Neurodevelopmental disorders, Nystagmus, Obsessive-compulsive disorder, Oligodactyly, Oral aversion, Phthisis bulbi, Physiologic amenorrhea, Prostatic neoplasms, Prostate cancer, Ptosis, Radioulnar synostosis, Renal insufficiency, Rhizomelia, Schizophrenia, Sleep apnea, Sleep disorders, Social communication disorder, Somatotropin deficiency, Speech disorders, Stereotyped behavior, Stomach neoplasms, Strabismus, Syndactyly of the toes, Synophrys, Talipes, Trigonocephaly, Uterine anomalies, Ventricular septal defect, Vesicoureteral reflux, Weaver syndrome, Wiedemann-steiner syndrome, Wrinkly skin syndromeView all (95 more) |
|
215
|
|
|
Keratinocyte proline rich protein |
C1orf45 |
|
|
216
|
|
|
Potassium two pore domain channel subfamily K member 4 |
FHEIG, K2p4.1, TRAAK, TRAAK1 |
|
|
217
|
|
|
Kelch like family member 5 |
- |
|
|
218
|
|
|
Lysine methyltransferase 5B |
CGI-85, CGI85, MRD51, SUV420H1 |
|
|
219
|
|
|
Potassium channel tetramerization domain containing 3 |
NY-REN-45 |
|
|
220
|
|
|
Potassium two pore domain channel subfamily K member 9 |
BIBARS, K2p9.1, KT3.2, TASK-3, TASK3, TASK32 |
Absence seizure, Akinetic petit mal, Birk-barel syndrome, Congenital finger flexion contractures, Developmental delay, Dolichocephaly, Dysphagia, Epilepsy, High palate, Mental retardation, Micrognathism, Mood disorder, Hypotonia, Spinal muscular atrophy, Submucous cleft of soft and hard palate |
