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Spondylometaphyseal dysplasia with dentinogenesis imperfecta

Also Known As:

Odontochondrodysplasia

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Stomatognathic Diseases: 705
- Tooth Diseases: 33
  - Tooth Abnormalities: 33
    - Dentinogenesis Imperfecta: 134
      - Spondylometaphyseal dysplasia with dentinogenesis imperfecta: 1
- Stomatognathic System Abnormalities
  - Tooth Abnormalities: 33
    - Dentinogenesis Imperfecta: 134
      - Spondylometaphyseal dysplasia with dentinogenesis imperfecta: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Stomatognathic System Abnormalities
    - Tooth Abnormalities: 33
      - Dentinogenesis Imperfecta: 134
        Spondylometaphyseal dysplasia with dentinogenesis imperfecta: 1
- Inborn Genetic Diseases: 11939
  - Osteochondrodysplasias: 592
    - Spondylometaphyseal dysplasia with dentinogenesis imperfecta: 1
Musculoskeletal Diseases: 719
- Bone Diseases: 5863
  - Developmental Bone Diseases: 153
    - Osteochondrodysplasias: 592
      - Spondylometaphyseal dysplasia with dentinogenesis imperfecta: 1

Related Diseases

1.	Hypophosphatemic Rickets
2.	Rickets (Rachitis)
3.	Osteogenesis Imperfecta (Lobstein Disease)
4.	Hypophosphatasia
5.	Ehlers-Danlos Syndrome (Syndrome, Ehlers-Danlos)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Spondylometaphyseal dysplasia with dentinogenesis imperfecta:

1.

Vitamin D FDA LinkGeneric

09/01/2023 - "Over 10 systemic diseases, including osteogenesis imperfecta, hypophosphatemic rickets, vitamin D-dependent rickets, familial tumoral calcinosis, Ehlers-Danlos syndrome, Schimke immuno-osseous dysplasia, hypophosphatasia, Elsahy-Waters syndrome, Singleton-Merten syndrome, odontochondrodysplasia, and microcephalic osteodysplastic primordial dwarfism type II were examined. "