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Brittle Cornea Syndrome (DOID:9005468)
Annotations: Rat: (3) Mouse: (3) Human: (3) Chinchilla: (3) Bonobo: (3) Dog: (3) Squirrel: (3) Pig: (3)
Parent Terms Term With Siblings Child Terms
corneal disease +     
Eye Abnormalities +     
Joint Instability +     
3MC syndrome 1  
ablepharon macrostomia syndrome  
Achard syndrome 
aniridia +   
Ankyloblepharon Filiforme Adnatum 
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anophthalmia +   
anterior segment dysgenesis +   
Arnold Stickler Bourne Syndrome 
arterial tortuosity syndrome  
Asymmetric Short Stature Syndrome 
Axenfeld-Rieger syndrome +   
Basel-Vanagaite-Smirin-Yosef syndrome  
blepharophimosis +   
blepharophimosis-intellectual disability syndrome, SBBYS type  
Blue Diaper Syndrome 
Bowman's membrane folds or rupture 
Brittle Cornea Syndrome +   
Cataract Microcornea Syndrome  
Chemke Oliver Mallek Syndrome 
chondrodysplasia with joint dislocations gPAPP type  
Choroidal Effusions +  
chromosome 6pter-p24 deletion syndrome 
CODAS syndrome  
Cole-Carpenter syndrome +   
coloboma +   
Colobomatous Macrophthalmia with Microcornea 
Combined Osteogenesis Imperfecta and Ehlers-Danlos Syndrome +   
Congenital Dislocation of Hip, with Hyperextensibility of Fingers and Facial Dysmorphism 
Congenital Nephrotic Syndrome with or without Ocular Abnormalities +   
cornea cancer +  
cornea plana +   
corneal argyrosis 
corneal degeneration +   
corneal deposit +  
corneal dystrophy +   
corneal ectasia 
corneal edema +   
Corneal Endothelial Cell Loss 
Corneal Graft Rejection  
Corneal Hypesthesia, Familial 
Corneal Injuries +   
corneal intraepithelial neoplasm 
corneal neovascularization +   
Corneal Opacity +   
corneal staphyloma 
Corneal Wavefront Aberration 
Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome  
Craniosynostosis with Ocular Abnormalities and Hallucal Defects 
cryptophthalmia +   
Cutaneous Hemangiomatosis with Associated Features 
Daish Hardman Lamont Syndrome 
De Hauwere syndrome 
Dermoids of Cornea 
Desanto-Shinawi Syndrome  
Desbuquois dysplasia +   
Diffuse Renal Mesangial Sclerosis, with Ocular Abnormalities 
Dwarfism Stiff Joint Ocular Abnormalities 
Ectopia Lentis +   
Egg-Shaped Pupil 
Ehlers-Danlos syndrome cardiac valvular type  
Ehlers-Danlos syndrome classic type 1  
Ehlers-Danlos syndrome classic type 2  
Ehlers-Danlos syndrome classic-like 1  
Ehlers-Danlos syndrome classic-like 2  
Ehlers-Danlos syndrome hypermobility type  
Ehlers-Danlos syndrome kyphoscoliotic type 1  
Ehlers-Danlos syndrome kyphoscoliotic type 2  
Ehlers-Danlos syndrome musculocontractural type 1  
Ehlers-Danlos syndrome musculocontractural type 2  
Ehlers-Danlos syndrome spondylodysplastic type 1  
Ehlers-Danlos syndrome spondylodysplastic type 2  
Ehlers-Danlos syndrome spondylodysplastic type 3  
Ehlers-Danlos Syndrome Type 4 +   
Ehlers-Danlos Syndrome Type 7 +   
Ehlers-Danlos Syndrome Type 8  
Ehlers-Danlos Syndrome VI Phenotype with Macrocephaly 
Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality 
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified 
Ehlers-Danlos Syndrome, Beasley Cohen Type 
Ehlers-Danlos Syndrome, Periodontal Type 2  
exudative vitreoretinopathy +   
FACES Syndrome 
Familial Joint Laxity +   
Familial Recurrent Dislocation of Patella 
Foveal Hypoplasia and Anterior Segment Dysgenesis  
Fronto-Facio-Nasal Dysplasia 
Frontoocular Syndrome 
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
Hernandez Aguirre-Negrete Syndrome 
hydrophthalmos +   
Hypospadias-Mental Retardation Syndrome 
iridogoniodysgenesis syndrome +   
Jaffer Beighton Syndrome 
Joubert syndrome 1  
Joubert Syndrome 2  
Joubert syndrome 9  
Kapur Toriello Syndrome 
keratitis +   
keratoconus +   
keratopathy +  
Maxillofacial Dysostosis 
megalocornea +   
Megarbane Syndrome 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Microcornea, Glaucoma, and Absent Frontal Sinuses 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
Microcornea, Rod-Cone Dystrophy, Cataract, and Posterior Staphyloma 1  
microphthalmia +   
Microspherophakia +   
MOMES Syndrome 
Nephrotic Syndrome with Ocular Anomalies 
Neuhauser Syndrome 
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
oblique facial clefting 1  
occipital horn syndrome  
oculoauricular syndrome  
Oculoauriculofrontonasal Syndrome 
Oculocerebrocutaneous Syndrome 
oculodentodigital dysplasia +   
Oculopalatocerebral Syndrome 
Oculorenocerebellar Syndrome 
Panic Disorder with Joint Laxity 
Pena Shokeir Syndrome Type 2 
persistent hyperplastic primary vitreous +   
PHACE Association  
Pierson syndrome  
popliteal pterygium syndrome +   
Prepapillary Vascular Loops 
pterygium +   
Pupillary Membrane, Persistence of 
Ramos Arroyo Clark Syndrome 
Retinal Dysplasia +   
ring dermoid of cornea  
Rozin Hertz Goodman Syndrome 
Schmid-Fraccaro Syndrome  
sclerocornea +   
spondyloepimetaphyseal dysplasia with joint laxity +   
Spondyloepiphyseal Dysplasia with Atlantoaxial Instability 
Stern Lubinsky Durrie Syndrome 
Stromme syndrome  
torsion dystonia with onset in infancy  
trachoma +   
Van Maldergem syndrome +   
X-linked cardiac valvular dysplasia  

Xrefs: OMIM:PS229200

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