Ehlers-Danlos syndrome type 5

Also Known As:

Ehlers-Danlos Syndrome, Type V

Networked: 3 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Cardiovascular Diseases: 91362
- Vascular Diseases: 15138
  - Hemostatic Disorders: 250
    - Ehlers-Danlos Syndrome: 799
      - Ehlers-Danlos syndrome type 5: 3
Hemic and Lymphatic Diseases: 6
- Hematologic Diseases: 3366
  - Hemorrhagic Disorders: 702
    - Hemostatic Disorders: 250
      - Ehlers-Danlos Syndrome: 799
        Ehlers-Danlos syndrome type 5: 3
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Skin Abnormalities: 159
    - Ehlers-Danlos Syndrome: 799
      - Ehlers-Danlos syndrome type 5: 3
- Inborn Genetic Diseases: 11939
  - Genetic Skin Diseases: 47
    - Ehlers-Danlos Syndrome: 799
      - Ehlers-Danlos syndrome type 5: 3
  - X-Linked Genetic Diseases: 42
    - Ehlers-Danlos syndrome type 5: 3
Skin and Connective Tissue Diseases
- Skin Diseases: 13127
  - Skin Abnormalities: 159
    - Ehlers-Danlos Syndrome: 799
      - Ehlers-Danlos syndrome type 5: 3
  - Genetic Skin Diseases: 47
    - Ehlers-Danlos Syndrome: 799
      - Ehlers-Danlos syndrome type 5: 3
- Connective Tissue Diseases: 3269
  - Collagen Diseases: 754
    - Ehlers-Danlos Syndrome: 799
      - Ehlers-Danlos syndrome type 5: 3

Related Diseases

1.	Osteogenesis Imperfecta (Lobstein Disease)
2.	Ehlers-Danlos Syndrome (Syndrome, Ehlers-Danlos)
3.	Cutis Laxa
4.	Type IV Ehlers-Danlos Syndrome
5.	Ehlers-Danlos syndrome type 6

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Ehlers-Danlos syndrome type 5:

1.	Protein-Lysine 6-Oxidase (Lysyl Oxidase)IBA 07/01/1982 - "One family with x-linked Ehlers-Danlos syndrome (type V) has been described with altered lysyl oxidase activity. " 01/01/1975 - "Lysyl oxidase deficiency in Ehlers-Danlos syndrome type V." 02/01/1976 - "Thus far, the primary heritable disorders of collagen metabolism in man include lysyl hydroxylase deficiency in Ehlers-Danlos syndrome type VI, p-collagen peptidase deficency in Ehlers-Danlos syndrome type VII, decreased synthesis of type III collagen in Ehlers-Danlos syndrome type IV, lysyl oxidase deficency in S-linked cutis laxa and Ehlers-Danlos syndrome type V, and decreased synthesis of type I collagen in osteogenesis imperfecta."
2.	Collagen Type III (Type III Collagen)IBA 02/01/1976 - "Thus far, the primary heritable disorders of collagen metabolism in man include lysyl hydroxylase deficiency in Ehlers-Danlos syndrome type VI, p-collagen peptidase deficency in Ehlers-Danlos syndrome type VII, decreased synthesis of type III collagen in Ehlers-Danlos syndrome type IV, lysyl oxidase deficency in S-linked cutis laxa and Ehlers-Danlos syndrome type V, and decreased synthesis of type I collagen in osteogenesis imperfecta."
3.	Collagen Type I (Type I Collagen)IBA 02/01/1976 - "Thus far, the primary heritable disorders of collagen metabolism in man include lysyl hydroxylase deficiency in Ehlers-Danlos syndrome type VI, p-collagen peptidase deficency in Ehlers-Danlos syndrome type VII, decreased synthesis of type III collagen in Ehlers-Danlos syndrome type IV, lysyl oxidase deficency in S-linked cutis laxa and Ehlers-Danlos syndrome type V, and decreased synthesis of type I collagen in osteogenesis imperfecta."
4.	Collagenases (Collagenase)FDA Link 02/01/1976 - "Thus far, the primary heritable disorders of collagen metabolism in man include lysyl hydroxylase deficiency in Ehlers-Danlos syndrome type VI, p-collagen peptidase deficency in Ehlers-Danlos syndrome type VII, decreased synthesis of type III collagen in Ehlers-Danlos syndrome type IV, lysyl oxidase deficency in S-linked cutis laxa and Ehlers-Danlos syndrome type V, and decreased synthesis of type I collagen in osteogenesis imperfecta."
5.	2-Oxoglutarate 5-Dioxygenase Procollagen-Lysine (Lysyl Hydroxylase)IBA 02/01/1976 - "Thus far, the primary heritable disorders of collagen metabolism in man include lysyl hydroxylase deficiency in Ehlers-Danlos syndrome type VI, p-collagen peptidase deficency in Ehlers-Danlos syndrome type VII, decreased synthesis of type III collagen in Ehlers-Danlos syndrome type IV, lysyl oxidase deficency in S-linked cutis laxa and Ehlers-Danlos syndrome type V, and decreased synthesis of type I collagen in osteogenesis imperfecta."
6.	CollagenIBA 02/01/1976 - "Thus far, the primary heritable disorders of collagen metabolism in man include lysyl hydroxylase deficiency in Ehlers-Danlos syndrome type VI, p-collagen peptidase deficency in Ehlers-Danlos syndrome type VII, decreased synthesis of type III collagen in Ehlers-Danlos syndrome type IV, lysyl oxidase deficency in S-linked cutis laxa and Ehlers-Danlos syndrome type V, and decreased synthesis of type I collagen in osteogenesis imperfecta."