|
821
|
|
|
TNF superfamily member 11 |
CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B, TRANCE, hRANKL2, sOdf |
Anemia, Congenital osteopetrosis, Cranial nerve paralysis, Craniosynostosis, Diaphyseal dysplasia, Facial paralysis, Hydrocephalus, Hypercalcemia, Lymphocytic leukemia, Macrocephaly, Malignant osteopetrosis, Malocclusion, Milk-alkali syndrome, Nystagmus, Opsoclonus, Optic atrophy, Mandibular osteomyelitis, Osteopetrosis, Osteoporosis, Otitis media, Pancytopenia, Periodontitis, Pulmonary arterial hypertension, RhinitisView all (9 more) |
|
822
|
|
|
Tumor protein p63 |
AIS, B(p51A), B(p51B), EEC3, KET, LMS, NBP, OFC8, RHS, SHFM4, TP53CP, TP53L, TP73L, p40, p51, p53CP, p63, p73H, p73L |
Absent lacrimal punctum, Accessory nipple, Adenocarcinoma, Adult syndrome, Hay-wells syndrome, Alopecia, Anaplastic carcinoma, Anhidrosis, Aniridia, Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome, Anonychia, Atresia of nasolacrimal duct, Bladder diverticulum, Bladder exstrophy, Blepharophimosis, Bowel incontinence, Breast diseases, Cafe-au-lait spot, Camptodactyly of fingers, Neoplasm, Carcinoma, Cervical cancer, Choanal atresia, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital abnormality of eustachian tube, Breast aplasia, Aplasia of the ovary, Congenital absent nipple, Congenital ankyloblepharon, Congenital anomaly of limb, Congenital camptodactyly, Congenital clubfoot, Congenital exomphalos, Congenital deformity of foot, Congenital anomaly of the hand, Breast hypoplasia, Pulmonary hypoplasia, Congenital hypoplasia of penis, Congenital hypoplasia of thymus, Congenital malrotation of intestine, Congenital omphalocele, Conjunctivitis, Corneal erosion, Corneal ulcer, Cryptorchidism, Dacryocystitis, Diabetes insipidus, Drachtman weinblatt sitarz syndrome, Dwarfism, Dysphagia, Ectodermal dysplasia, Ectrodactyly, Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome, Eczema, Endocrine breast diseases, Entropion, Epispadias, Female urogenital diseases, Fingernail dysplasia, Neck cancer, Hearing loss, Hydronephrosis, Hyperkeratosis, Hypodontia, Hypogonadotropic hypogonadism, Hypohidrosis, Hypohidrotic ectodermal dysplasia, Hypoplasia of nipple, Hypoplasia of the maxilla, Hypospadias, Hypothyroidism, Hypotrichosis, Isolated somatotropin deficiency, Isolated split hand-split foot malformation, Keratitis, Limb-mammary syndrome, Lung neoplasms, Lung adenocarcinoma, Lung cancer, Lung carcinoma, Lymphoma, Lymphoblastic leukemia, Macrodontia, Malnutrition, Melanocytic nevus, Mental retardation, Microdontia, Micrognathism, Microstomia, Microtia, Multiple congenital anomalies, Nail diseases, Nail dysplasia, Nail dystrophy, Nevus, Non-alcoholic fatty liver disease, Oligodactyly, Oligodontia, Onychogryposis, Oral cleft, Oropharyngeal dysphagia, Orofacial cleft, Otitis media, Ovarian neoplasm, Ovarian cancer, Palmoplantar keratoderma, Pancreatic neoplasm, Pancreatic carcinoma, Pancreatic cancer, Patent ductus arteriosus, Peg-shaped teeth, Penis agenesis, Physiologic amenorrhea, Premature menopause, Biliary cirrhosis, Psoriasiform eczema, Ptosis, Rapp-hodgkin syndrome, Renal agenesis, Renal dysplasia, Rudiger syndrome, Sensorineural hearing loss, Situs inversus, Somatotropin deficiency, Specific learning disorder, Split hand foot deformity, Split-hand-foot malformation, Submucosal cleft palate, Submucous cleft of soft and hard palate, Sweat gland neoplasms, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Taurodontism, Ureterocele, Urethral atresia, Velopharyngeal insufficiency, Ventricular septal defect, Vesicoureteral refluxView all (126 more) |
|
823
|
|
|
Tyrosine kinase non receptor 1 |
KOS1 |
|
|
824
|
|
|
TNF superfamily member 14 |
CD258, HVEML, LIGHT, LTg |
|
|
825
|
|
|
TNF superfamily member 13 |
APRIL, CD256, TALL-2, TALL2, TNLG7B, TRDL-1, UNQ383/PRO715, ZTNF2 |
|
|
826
|
|
|
TNF superfamily member 12 |
APO3L, DR3LG, TNF12, TNLG4A, TWEAK |
Anemia, Atrial fibrillation, Brachycephaly, Bronchiectasis, Bronchitis, Common variable immunodeficiency, Gastrointestinal stromal tumor, Immune thrombocytopenic purpura, Immunologic deficiency syndromes, Imperforate anus, Lymphoma, Lymphopenia, Otitis media, Paroxysmal atrial fibrillation, Vasculitis |
|
827
|
|
|
TNF superfamily member 10 |
APO2L, Apo-2L, CD253, TANCR, TL2, TNLG6A, TRAIL |
Breast cancer, Mammary neoplasms, Breast carcinoma, Chromophobe carcinoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Endometrial neoplasms, Endometrial carcinoma, Giant cell glioblastoma, Glioblastoma, Glioma, Kidney neoplasm, Kidney cancer, Leukemia, Liver neoplasms, Liver cancer, Liver carcinoma, Lung adenocarcinoma, Marfan syndrome, Miscarriage, Myeloid leukemia, Neuroblastoma, Ovarian neoplasm, Ovarian cancer, Pancreatic neoplasm, Pancreatic cancer, Papillary renal carcinoma, Prostatic neoplasms, Prostate cancer, Renal carcinomaView all (16 more) |
|
828
|
|
|
TNF superfamily member 9 |
4-1BB-L, CD137L, TNLG5A |
|
|
829
|
|
|
TNF receptor superfamily member 14 |
ATAR, CD270, HVEA, HVEM, LIGHTR, TR2 |
|
|
830
|
|
|
TNF receptor superfamily member 6b |
DCR3, DJ583P15.1.1, M68, M68E, TR6 |
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