601
|
|
|
ATPase copper transporting beta |
PWD, WC1, WD, WND |
Anaplastic carcinoma, Anemia, Arthritis, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Carcinoma of the head and neck, Chondrocalcinosis, Cirrhosis, Colorectal cancer, Colorectal neoplasms, Dementia, Dysarthria, Dyslipidemias, Dysphagia, Epileptic encephalopathy, Esophageal varix, Fatty liver, Hepatolenticular degeneration, Hypersexuality, Hypoparathyroidism, Kayser-fleischer ring, Kidney neoplasm, Kidney cancer, Liver neoplasms, Liver cancer, Liver cirrhosis, Liver failure, Liver fibrosis, Marfan syndrome, Mental depression, Mental retardation, Mixed demyelinating and axonal polyneuropathy, Mouth neoplasms, Malignant neoplasm of mouth, Nephrolithiasis, Osteoporosis, Ovarian neoplasm, Ovarian cancer, Phosphate diabetes, Prostatic neoplasms, Prostate cancer, Renal tubular disorder, Rickets, Wilson diseaseView all (31 more) |
602
|
|
|
Anillin, actin binding protein |
FSGS8, Scraps, scra |
|
603
|
|
|
ATPase family AAA domain containing 2B |
- |
|
604
|
|
|
Ankyrin repeat and IBR domain containing 1 |
- |
|
605
|
|
|
ATR checkpoint kinase |
FCTCS, FRP1, MEC1, SCKL, SCKL1 |
Alopecia, Benign neoplasm of stomach, Blepharophimosis, Camptodactyly of fingers, Clinodactyly, Dislocated radial head, Craniosynostosis, Cryptorchidism, Dental enamel hypoplasia, Dwarfism, Elbow flexion contracture, Endometrial cancer, Endometrial carcinoma, Glaucoma, Glioma, High palate, Hypertrophy of clitoris, Hypospadias, Impaired cognition, Infiltrating duct carcinoma of female breast, Lung carcinoma, Lung adenocarcinoma, Malignant neoplasm, Mental retardation, Microcephaly, Micrognathism, Myeloproliferative disorder, Ovarian neoplasm, Ovarian cancer, Ovarian carcinoma, Pachygyria, Pancytopenia, Prostatic neoplasms, Prostate cancer, Scoliosis, Seckel syndrome, Oropharyngeal carcinoma, Stomach neoplasms, Stomach carcinoma, Strabismus, Talipes, Telangiectasia and cancer syndrome, Telangiectasia and oropharyngeal cancer predisposition syndrome, Urinary tract cancer, Urologic neoplasmsView all (30 more) |
606
|
|
|
ADAMTS like 4 |
ADAMTSL-4, ECTOL2, TSRC1 |
|
607
|
|
|
Amyloid beta precursor protein binding family B member 1 interacting protein |
INAG1, PREL1, RARP1, RIAM |
|
608
|
|
|
Ankyrin repeat domain 16 |
- |
|
609
|
|
|
ATRX chromatin remodeler |
JMS, MRX52, RAD54, RAD54L, XH2, XNP, ZNF-HX |
Absent mastoid, Alpha-thalassemia myelodysplasia syndrome, Acquired kyphoscoliosis, Adenocarcinoma, Agenesis of corpus callosum, Alpha-thalassemia mental retardation syndrome, x-linked, Alpha-thalassemia-myelodysplastic syndrome, Ambiguous genitalia, Anemia, Anorexia, Aplasia cutis congenita, Autism, Bilateral renal hypoplasia, Brachycephaly, Brachydactyly, Bronchospasm, Camptodactyly of fingers, Cerebral atrophy, Cerebral cortical atrophy, Clinodactyly, Asplenia, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Congenital kyphoscoliosis, Congenital pectus carinatum, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Dysmorphic features, Dysphasia, Encephalitis, Exotropia, Gastroesophageal reflux disease, Glioblastoma, Glioma, Hearing loss, Heart failure, High palate, Hirschsprung disease, Hydronephrosis, Hypogonadism, Hypospadias, Immunologic deficiency syndromes, Mental retardation, Intestinal volvulus, Iron deficiency anemia, Juberg-marsidi syndrome, Leukemia, Spastic diplegia, Liver failure, Lumbar scoliosis, Macroglossia, Macrostomia, Male pseudohermaphroditism, Malocclusion, Mental depression, Microcephaly, Micrognathism, Microtia, Movement disorders, Multiple congenital anomalies, Myelodysplasia, Myelodysplastic syndrome, Myopia, Neuroblastoma, Neuroendocrine tumor of stomach, Neuroendocrine tumors, Neutropenia, Obesity, Optic atrophy, Osteosarcoma, Pancreatic endocrine carcinoma, Pancreatic neoplasm, Pancreatic cancer, Paraganglioma, Penile diseases, Penis agenesis, Posteriorly rotated ear, Ptosis, Pulmonary carcinoid tumor, Renal agenesis, Renal hypoplasia, Spastic paraplegia, Stereotyped behavior, Thoracic diseases, Thyroglossal cyst, Tricuspid valve insufficiency, Postaxial hand polydactyly, Ventricular failure, Ventricular septal defect, Vesicoureteral reflux, Zollinger-ellison syndromeView all (80 more) |
610
|
|
|
ARF like GTPase 15 |
ARFRP2 |
|