type 3 Rhizomelic chondrodysplasia punctata

Also Known As:

Rhizomelic chondrodysplasia punctata, type 3; AGPS deficiency; Alkyldihydroxyacetonephosphate synthase deficiency; Alkylglycerone-Phosphate Synthase Deficiency

Musculoskeletal Diseases: 719
- Bone Diseases: 5863
  - Developmental Bone Diseases: 153
    - Osteochondrodysplasias: 592
      - Chondrodysplasia Punctata: 178
        Rhizomelic Chondrodysplasia Punctata: 112
        type 3 Rhizomelic chondrodysplasia punctata: 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Peroxisomal Disorders: 504
      - Rhizomelic Chondrodysplasia Punctata: 112
        type 3 Rhizomelic chondrodysplasia punctata: 2
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Peroxisomal Disorders: 504
      - Rhizomelic Chondrodysplasia Punctata: 112
        type 3 Rhizomelic chondrodysplasia punctata: 2

Ryan P Liegel Selected Research

Ryan P Liegel Research Topics

Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure