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Term:
Connective tissue disease with eye involvement (EFO:Orphanet:98702)
Annotations: Rat: (0) Mouse: (0) Human: (237) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
benign connective and soft tissue neoplasm +   
Blindness-scoliosis-arachnodactyly syndrome 
Central cloudy dystrophy of Francois 
collagenopathy +  
Connective tissue disease with eye involvement +   
connective tissue neoplasm +   
Corneal dystrophy - perceptive deafness 
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis 
Ectodermal malformation syndrome associated with ocular features +  
enthesopathy +   
Familial amyloidosis, Finnish type 
fasciitis +  
fibroblastic disorder 
Fuchs endothelial corneal dystrophy  
Genetic developmental defect of the eye +  
Genetic lens and zonula anomaly +  
Genetic neuro-ophthalmological disease +  
Genetic vitreous-retinal disease +  
Genodermatosis with ocular features +  
hereditary disorder of connective tissue +   
interstitial cystitis 
ligament rupture  
linkeropathy +  
Metabolic disease associated with ocular features +  
Microcystic corneal dystrophy 
myxosarcoma 
Optic neuropathy +  
overlapping connective tissue disease +   
panniculitis +  
periostitis 
Rare disease with glaucoma as a major feature +  
Rare genetic palpebral, lacrimal system and conjunctival disease +  
Rare genetic refraction anomaly +  
Reis-Bücklers corneal dystrophy 
rheumatic disease +   
Spastic ataxia - corneal dystrophy 
Subaortic stenosis - short stature 
synovitis +  
Tendinopathy +   
X-linked reticulate pigmentary disorder with systemic manifestations 

Synonyms
Xrefs: MIM:614170 ;   ORDO:98702 ;   UMLS:C0009782

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