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Nosology (Classifications) of Osteogenesis Imperfecta
OI TYPE |
INHERITANCE |
PHENOTYPE |
GENE MUTATION |
DEFECTS IN COLLAGEN SYNTHESIS, STRUCTURE, OR PROCESSING |
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I |
AD |
Mild |
Null COL1A1 Allele |
II |
AD |
Lethal |
COL1A1 or COL1A2 |
III |
AD |
Progressive Deforming |
COL1A1 or COL1A2 |
IV |
AD |
Moderate |
COL1A1 or COL1A2 |
XIII |
AR |
Mild/Severe |
BMP1 |
DEFECTS IN BONE MINERALIZATION |
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V |
AR |
Variable, Distinctive Histology |
IFITM5 |
VI |
AR |
Moderate/Severe |
SERPINF1 |
DEFECTS IN COLLAGEN MODIFICATION |
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VII |
AR |
Severe (Hypomorphic) Severe/Lethal (Null) |
CRTAP |
VIII |
AR |
Severe/Lethal |
LEPRE1 |
IX |
AR |
Moderate/Lethal |
PPIB |
XIV |
AR |
Severe |
TMEM38B |
DEFECTS IN COLLAGEN FOLDING AND CROSS-LINKING |
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X |
AR |
Severe/Lethal |
SERPINH1 |
XI/BRKS1 |
AR |
Mild/Severe |
FKBP10 |
BRKS2 |
AR |
Moderate/Severe |
PLOD2 |
DEFECTS IN OSTEOBLAST DEVELOPMENT WITH COLLAGEN INSUFFICIENCY |
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XII |
AR |
Severe |
SP7 |
XV |
AR |
Severe |
WNT1 |
XVI |
AR |
Severe |
CREB3L1 |
XVII |
AR |
Progressive Severe |
SPARC |
XVIII |
XR |
Moderate/Severe |
MBTPS2 |
XIX |
AR |
Severe |
FAM46A/TENT5A |
XX |
AR |
Progressive Severe/Lethal |
MESD |
XXI |
AR |
Severe + Neurodevelopmental |
KDELR2 |
XXII |
AR |
Severe |
CCDC134 |
Abbreviations:
AD = autosomal dominant; the mutation is inherited in a dominant manner AR = autosomal recessive; the mutation is inherited in a recessive manner