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1.

Osteogenesis imperfecta type 9

Osteogenesis imperfecta (OI) is a connective tissue disorder characterized clinically by bone fragility and increased susceptibility to fractures. Osteogenesis imperfecta type IX (OI9) is a severe autosomal recessive form of the disorder (summary by van Dijk et al., 2009). [from OMIM]

MedGen UID:
376720
Concept ID:
C1850169
Disease or Syndrome
2.

Hip joint hypermobility

MedGen UID:
658643
Concept ID:
C0574977
Finding

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