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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Brittle Cornea Syndrome +   
Combined Osteogenesis Imperfecta and Ehlers-Danlos Syndrome +   
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 classic-like 3  
This disease is an autosomal dominant connective tissue disorder characterized by joint hypermobility and frequent joint dislocations, atrophic scarring, prolonged bleeding time, and age-related aortic dilatation and rupture.
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 periodontal type 1  
Ehlers-Danlos syndrome periodontal 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 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 
Hernandez Aguirre-Negrete Syndrome 
occipital horn syndrome  
X-linked cardiac valvular dysplasia  

Synonyms
Exact Synonyms: EDSCLL3 ;   EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 3 ;   Ehlers-Danlos syndrome classic-like type 3
Primary IDs: OMIM:620865
Definition Sources: OMIM:620865

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