FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Ehlers-Danlos syndrome dermatosparaxis type ID (Ontology) DOID:0080733 (Human Disease)
Definition An Ehlers-Danlos syndrome that is characterized by severe skin fragility, sagging, redundant skin and that has_material_basis_in mutation in the gene encoding the procollagen protease ADAMTS2 on chromosome 5q35.
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 Genes
 Ehlers-Danlos syndrome dermatosparaxis type       1
 for disease ribbon | Ehlers-Danlos syndrome dermatosparaxis type       1
 model of | Ehlers-Danlos syndrome dermatosparaxis type       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
collagen disease                 |
 |__Ehlers-Danlos syndrome_______|
                                 Ehlers-Danlos syndrome dermatosparaxis type  1 rec.
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Is a autosomal recessive disease
Ehlers-Danlos syndrome
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MIM:225410