Disease Browser
Parent Node: Eye Abnormalities (D005124) ..Starting node .. Axenfeld-Rieger syndrome (C535679) Child Nodes:
........AXENFELD-RIEGER SYNDROME, TYPE 1 (OMIM:180500) ........AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499) ........AXENFELD-RIEGER SYNDROME, TYPE 3 (OMIM:602482) Sister Nodes: ..Ablepharon macrostomia syndrome (C535557) ..Aniridia (D015783) 10 ..Ankyloblepharon filiforme adnatum cleft palate (C536373) ..Anophthalmos (D000853) 8 ..Anterior segment mesenchymal dysgenesis (C537775) ..Asymmetric Short Stature Syndrome (C566248) ..Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss (C537789) ..Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234) ..Axenfeld-Rieger syndrome (C535679) 3 ..Blepharophimosis (D016569) 17 ..Blue diaper syndrome (C536239) ..Brachymetapody-Anodontia-Hypotrichosis-Albinoidism (C565893) ..Chemke Oliver Mallek syndrome (C535922) ..Chromosome 6pter-P24 Deletion Syndrome (C567239) ..CODAS syndrome (C536434) ..Cole Carpenter syndrome (C535963) ..Coloboma (D003103) 43 ..Craniosynostosis with Ocular Abnormalities and Hallucal Defects (C564263) ..Cryptophthalmos, Unilateral or Bilateral, Isolated (C565138) ..Dwarfism stiff joint ocular abnormalities (C535724) ..Ectopia Lentis (D004479) 13 ..FACES syndrome (C536384) ..Foveal Hypoplasia and Anterior Segment Dysgenesis (C563774) ..Fraser Syndrome (D058497) ..Fronto-facio-nasal dysplasia (C538063) ..Frontoocular Syndrome (C565340) ..Goniodysgenesis-Mental Retardation-Short Stature Syndrome (C564214) ..Hay-Wells syndrome (C535847) ..Hydrophthalmos (D006871) ..Iridogoniodysgenesis and skeletal anomalies (C535534) ..Iridogoniodysgenesis type1 (C535535) ..Iridogoniodysgenesis, dominant type (C535536) ..Jejunal Atresia with Microcephaly and Ocular Anomalies (C565460) ..Joubert syndrome 1 (C536293) ..Joubert syndrome 2 (C536294) ..Joubert Syndrome 9 (C567364) ..Kapur Toriello syndrome (C537008) ..Kaufman oculocerebrofacial syndrome (C537013) ..Macrophthalmia, Colobomatous, with Microcornea (C566533) ..Maxillofacial Dysostosis (C563599) ..Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities (C565405) ..Microcornea, glaucoma, and absent frontal sinuses (C537552) ..Microphthalmos (D008850) 57 ..MOMES Syndrome (C564660) ..Nephrotic syndrome ocular anomalies (C536403) ..Nephrotic Syndrome, Congenital, with or without Ocular Abnormalities (C563805) ..Oculoauricular Syndrome (C567416) ..Oculoauriculofrontonasal syndrome (C537865) ..Oculocerebrocutaneous syndrome (C538088) ..Oculodentodigital Dysplasia (C563160) ..Oculodentodigital Dysplasia, Autosomal Recessive (C567605) ..Oculomaxillofacial dysostosis (C537736) ..Oculopalatocerebral Syndrome (C564935) ..Oculopalatoskeletal syndrome (C537738) ..Oculorenocerebellar syndrome (C537739) ..Pena Shokeir syndrome Type 2 (C536646) ..Persistent Hyperplastic Primary Vitreous (D054514) ..Persistent Hyperplastic Primary Vitreous, Autosomal Recessive (C566966) ..Peters anomaly (C537884) ..PHACE association (C537892) ..Pierson syndrome (C537185) ..Popliteal Pterygium Syndrome (C562509) ..Popliteal Pterygium Syndrome, Lethal Type (C564874) ..Prepapillary Vascular Loops (C563287) ..Pupil, Egg-Shaped (C566731) ..Pupillary Membrane, Persistence Of (C562700) ..Retinal Dysplasia (D015792) 2 ..Rieger syndrome 2 (C535680) ..Rozin Hertz Goodman syndrome (C535876) ..Torsion dystonia with onset in infancy (C536969) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD