Select Entries from OMIM -- Online Mendelian Inheritance in Man

Select Entries from OMIM --Online Mendelian Inheritance in Man

60 entries found, searching for "congenital glaucoma"

#231300 GLAUCOMA 3, PRIMARY INFANTILE, A; GLC3A
*600975 GLAUCOMA 3, PRIMARY INFANTILE, B; GLC3B
229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA
#137750 GLAUCOMA 1, OPEN ANGLE, A; GLC1A
*601771 CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 1; CYP1B1
*156600 MICROCORIA, CONGENITAL
#601631 IRIDOGONIODYSGENESIS, TYPE 1; IRID1
#137600 IRIDOGONIODYSGENESIS, TYPE 2; IRID2
*277600 WEILL-MARCHESANI SYNDROME
187501 TETRALOGY OF FALLOT AND GLAUCOMA
#604278 RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH BILATERAL GLAUCOMA, CATARACTS, AND BAND KERATOPATHY
*602669 PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR 3; PITX3
*231500 GLAUCOMA, JUVENILE
*601090 FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 7; FKHL7
*601682 GLAUCOMA 1, OPEN ANGLE, C; GLC1C
*106210 PAIRED BOX GENE 6; PAX6
600252 LOWRY-MACLEAN SYNDROME
*236670 WALKER-WARBURG SYNDROME
#161200 NAIL-PATELLA SYNDROME; NPS
269880 SHORT SYNDROME
249420 MELNICK-NEEDLES SYNDROME
#180849 RUBINSTEIN SYNDROME
*162200 NEUROFIBROMATOSIS, TYPE I; NF1
#180500 RIEGER SYNDROME, TYPE 1; RIEG1
*251600 MICROPHTHALMOS, AUTOSOMAL RECESSIVE
*122000 CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR
*129600 ECTOPIA LENTIS, ISOLATED
*220210 DANDY-WALKER-LIKE MALFORMATION WITH ATRIOVENTRICULAR SEPTAL DEFECT
#154700 MARFAN SYNDROME; MFS
#109400 BASAL CELL NEVUS SYNDROME; BCNS
*253280 MUSCLE-EYE-BRAIN DISEASE; MEB
*236200 HOMOCYSTINURIA
219250 CUTIS MARMORATA TELANGIECTATICA CONGENITA; CMTC
*143200 HYALOIDEORETINAL DEGENERATION OF WAGNER
*601499 RIEGER SYNDROME, TYPE 2; RIEG2
211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS
*123580 CRYSTALLIN, ALPHA-A; CRYAA
300166 OCULOFACIOCARDIODENTAL SYNDROME
#269000 SC PHOCOMELIA SYNDROME
*274000 THROMBOCYTOPENIA--ABSENT RADIUS SYNDROME
*213600 FAHR DISEASE
*251450 MICROMELIC DWARFISM WITH VERTEBRAL AND METAPHYSEAL ABNORMALITIES AND ADVANCED CARPOTARSAL OSSIFICATION
208300 ASCITES, CHYLOUS
#225400 EHLERS-DANLOS SYNDROME, TYPE VI
*264900 PTA DEFICIENCY
185300 STURGE-WEBER SYNDROME
#176270 PRADER-WILLI SYNDROME; PWS
206750 ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTOR RETARDATION
*309801 MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS
*259770 OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG
*123570 CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED
236750 HYDROPS FETALIS, IDIOPATHIC
#108300 STICKLER SYNDROME, TYPE I; STL1
#106200 ANIRIDIA; AN1
600776 ANOPHTHALMIA-PLUS SYNDROME
*261540 PETERS ANOMALY WITH SHORT-LIMB DWARFISM
224400 DYSSEGMENTAL DWARFISM
#154780 MARSHALL SYNDROME
149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME
*603474 RIBOSOMAL PROTEIN S19; RPS19