Select Entries from OMIM -aniridia

Select Entries from OMIM -- Online Mendelian Inheritance in Man

33 entries found, searching for "aniridia"

*106210 PAIRED BOX GENE 6; PAX6
#106200 ANIRIDIA; AN1
*206700 ANIRIDIA, CEREBELLAR ATAXIA, AND MENTAL DEFICIENCY
#194072 WAGR SYNDROME
106220 ANIRIDIA AND ABSENT PATELLA
106230 ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT
206750 ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTOR RETARDATION
*194070 WILMS TUMOR 1; WT1
*115500 CATALASE; CAT
#137357 GENITOURINARY DYSPLASIA COMPONENT OF WAGR SYNDROME; GUD
*190020 V-HA-RAS HARVEY RAT SARCOMA VIRAL ONCOGENE HOMOLOG; HRAS
*136530 FOLLICLE-STIMULATING HORMONE, BETA POLYPEPTIDE; FSHB
#171300 PHEOCHROMOCYTOMA
*151250 LETHAL ANTIGEN--A1; AL-A1
#148190 KERATITIS, HEREDITARY
156190 MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA
#129750 ECTOPIA PUPILLAE
#136520 FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROME
*143040 ANTIGEN DEFINED BY MONOCLONAL ANTIBODY F10.44.2
#115470 CAT EYE SYNDROME; CES
234100 HALLERMANN-STREIFF SYNDROME; HSS
245450 LACTIC ACIDURIA DUE TO D-LACTIC ACID
*602942 NEUROBLASTOMA STAGE 4S GENE
603807 PETERS ANOMALY WITH CATARACT
*142460 SYNDECAN 2; SDC2
*133701 EXOSTOSES, MULTIPLE, TYPE II
*185440 SUPPRESSOR OF TUMORIGENICITY 2; ST2
*183600 SPLIT-HAND/FOOT MALFORMATION, TYPE 1; SHFM1
210350 BIEMOND SYNDROME II
*212500 CATARACT, CONGENITAL OR JUVENILE
*600911 CHROMOSOME 11 OPEN READING FRAME 8; C11ORF8
*601881 RX HOMEO BOX GENE
*602504 SHORT STATURE HOMEO BOX 2; SHOX2