PomBase home

Disease association ontology term - MONDO:0020066 - Ehlers-Danlos syndrome

Term summary

ID
MONDO:0020066
Name
Ehlers-Danlos syndrome
Ontology or CV name
Disease association
Definition
The Ehlers–Danlos syndromes (EDS) are a clinically and genetically heterogeneous group of heritable connective tissue disorders (HCTDs) characterized by joint hypermobility, skin hyperextensibility, and tissue fragility.

Parents

Annotation

Disease association

MONDO:0020066 - Ehlers-Danlos syndrome

References:

Genes:

MONDO:0016002 - Ehlers-Danlos syndrome, kyphoscoliotic type 1

References:

Genes:

MONDO:0013800 - Ehlers-Danlos syndrome, kyphoscoliotic type, 2

References:

Genes:

MONDO:0012873 - Ehlers-Danlos syndrome, spondylocheirodysplastic type

References:

Genes:

MONDO:0014139 - Ehlers-Danlos syndrome, spondylodysplastic type, 2

References:

Genes: