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Term:
Anterior Segment Dysgenesis 4 (DOID:9004838)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
glaucoma +     
iris disease +     
Absent Eyebrows and Eyelashes with Mental Retardation 
Ackerman Syndrome 
angle-closure glaucoma +   
aniridia +   
anodontia +   
Anterior Segment Dysgenesis 1  
Anterior Segment Dysgenesis 3  
Anterior Segment Dysgenesis 4  
Anterior Segment Dysgenesis 6  
Anterior Segment Dysgenesis 7  
Anterior Segment Dysgenesis 8  
aqueous misdirection 
AREDYLD Syndrome 
blepharocheilodontic syndrome +   
Book Syndrome 
borderline glaucoma +  
Bowen Syndrome 
Carabelli Anomaly of Maxillary Molar Teeth 
ciliary body disease +  
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only  
CODAS syndrome  
congenital aphakia  
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Congenital Deafness, and Onychodystrophy, Autosomal Dominant  
Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome  
Craniosynostosis and Dental Anomalies  
De Hauwere Leroy Adriaenssens syndrome 
Dens in Dente +  
dental enamel hypoplasia +   
dentin dysplasia +   
dentinogenesis imperfecta +   
Dermoodontodysplasia 
Diastema +  
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Dyssegmental Dysplasia with Glaucoma 
Early-Onset Glaucoma +   
Edict Syndrome  
Euhidrotic Ectodermal Dysplasia 
exfoliation syndrome  
Faciocardiomelic Dysplasia, Lethal 
Friedreich Ataxia Congenital Glaucoma 
Fused Teeth 
GEMSS Syndrome  
Ghose Sachdev Kumar Syndrome 
Glaucoma 1, Open Angle, O +   
Glaucoma 3, Primary Congenital, C 
Glaucoma 3, Primary Congenital, D  
Glaucoma 3, Primary Congenital, E  
Glaucoma 3, Primary Infantile, B  
Glaucoma and Sleep Apnea 
glaucomatous atrophy of optic disc 
Grubben de Cock Borghgraef Syndrome 
Heterochromia Iridis  
hypersecretion glaucoma 
Hypoglossia-Hypodactylia 
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
Iridocorneal Endothelial Syndrome +  
iridocyclitis +   
Iridogoniodysgenesis and Skeletal Anomalies 
Iris Hypoplasia and Glaucoma  
Iris Neoplasms +  
iritis 
KBG syndrome  
LADD syndrome  
Larsen syndrome  
Lowry Maclean syndrome 
MacKay Shek Carr Syndrome 
Microcornea, Glaucoma, and Absent Frontal Sinuses 
Microspherophakia +   
Nance-Horan syndrome  
neovascular glaucoma  
Normal Tension Glaucoma  
oculodentodigital dysplasia +   
Oculoskeletodental Syndrome  
Oculotrichodysplasia 
Odontodysplasia +   
Odontomicronychial Dysplasia 
Odontotrichoungual-Digital-Palmar Syndrome 
open-angle glaucoma +   
Oroacral Syndrome, Verloes-Koulischer Type 
Otodental Dysplasia 
Peters anomaly +   
Peters Anomaly with Cataract 
phacogenic glaucoma +   
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
primary congenital glaucoma +   
Proximal Renal Tubular Acidosis, with Ocular Abnormalities and Mental Retardation  
Rodrigues Blindness 
Spastic Paresis, Glaucoma, and Mental Retardation 
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition 
steroid-induced glaucoma +  
Supernumerary Tooth +  
Taurodontism +  
Taurodontism, Microdontia, and Dens Invaginatus 
Teeth Noneruption of with Maxillary Hypoplasia and Genu Valgum 
Teeth, Odd Shapes of 
temtamy preaxial brachydactyly syndrome  
Tetralogy of Fallot and Glaucoma 
tooth agenesis +   
traumatic glaucoma 
Tricho-Dento-Osseous Syndrome 1 
Weyers Acrofacial Dysostosis  
Zazam Sheriff Phillips Syndrome 

Synonyms
Exact Synonyms: ASGD4 ;   IHGA ;   IRID 2 ;   IRID2 ;   Iris hypoplasia with early onset glaucoma, autosomal dominant ;   iridogoniodysgenesis type 2
Primary IDs: MESH:C535536
Alternate IDs: OMIM:137600 ;   RDO:0000708

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.