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Longitudinal deficiency, fibular, complete or partial with or without distal deficiencies, incomplete
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DISO:MTHICD9 |
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Longitudinal deficiency, fibular, complete or partial
|
DISO:MTHICD9 |
|
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Longitudinal deficiency, tarsals or metatarsals, complete or partial with or without incomplete phalangeal deficiency
|
DISO:MTHICD9 |
|
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Longitudinal deficiency, tarsals or metatarsals, complete or partial
|
DISO:MTHICD9 |
|
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Other congenital anomalies of spine
|
DISO:MTHICD9 |
|
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Other congenital osteodystrophies
|
DISO:MTHICD9 |
|
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Other specified congenital anomalies of muscle, tendon, fascia, and connective tissue
|
DISO:MTHICD9 |
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Other and unspecified congenital anomalies of musculoskeletal system
|
DISO:MTHICD9 |
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Specified congenital anomalies of nails
|
DISO:MTHICD9 |
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Xeroderma pigmentosum, group F
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DISO:MTH |
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Osteogenesis imperfecta, dominant perinatal lethal
|
DISO:MTH |
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Osteogenesis imperfecta type IV (disorder)
|
DISO:MTH |
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Childhood hypophosphatasia (disorder)
|
DISO:MTH |
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Brown oculocutaneous albinism
|
DISO:MTH |
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