Disease staging: CliniCal anD CoDeD Criteria - HCUP

Clinical Criteria with Description, Diagnostic Findings and ICD-9-CM codes
DXCat Number: MUS35
MultiStage: No
DXCat Label: Osteochondrodysplasia Specificity: A
Etiology: Genetic (or hereditary)
Stage Description Diagnostic findings ICD-9-CM Codes
1.01 Osteochondrodysplasia Achondroplasia [ physical examination or genetic analysis report defect in chromosome 4p]
DX 7564, 75655, 75656, 75659,
OR hypochondroplasia [physical examination or genetic analysis report]
7569;
OR pseudoachondroplasia [physical examination or genetic analysis report]
OR diastrophic dysplasia [physical examination or genetic analysis report]
OR multiple epiphyseal dysplasia [physical examination or genetic analysis report]
OR spondyloepiphyseal dysplasia [physical examination or genetic analysis report]
OR metaphyseal chondrodysplasia [physical examination or genetic analysis report]
OR mesomelic dysplasia [physical examination or genetic analysis report]
OR chondrodysplasia punctata, rhizomelic form [physical examination or genetic analysis
report
OR chondrodysplasia punctata, Conradi-Hünermann form [physical examination or genetic
analysis report]
OR chondroectodermal dysplasia [physical examination or genetic analysis report]
2.01 with hydrocephalus Stage 1.01
AND hydrocephalus [physical examination or CT scan report]
2.02 with mental retardation Stage 1.01-2.01
AND mental retardation:
3.01 with respiratory failure Stage 1.01-2.02
AND respiratory failure:
3.02 with coma Stage 1.01-3.01
AND coma:
3.03 with shock Stage 1.01-3.02
AND shock:
4.00 with death Stage 1.01-3.03
AND death
STAGE 1.01 + (DX 3314, 7423);
STAGE 1.01-2.01 + DXCAT NEU15;
STAGE 1.01-2.02 + GROUP
RESP_FAIL;
STAGE 1.01-3.01 + GROUP COMA;
STAGE 1.01-3.02 + (GROUP
SHOCKC OR GROUP SHOCKN) ;
NO;
References:
Krane SM, Schiller AL. Polyostotic fibrous dysplasia, hyperostosis and other disorders of bone and metabolism. In: Fauci AS, Braunwald E, Isselbacher KJ, Wilson JD, Martin JB,
Kasper DL, Hauser SL, Longo DL, eds. Harrison's Principles of Internal Medicine. 14th ed. New York, NY: McGraw-Hill; 1998:2269-2277.
Newbury-Ecob R. Atelosteogenesis type 2. Journal of Medical Genetics. 1998;35(1):49-53.
Ozaki T, Lindner N, Blasius S. Dedifferentiated chondrosarcoma in Albright syndrome. A case report and review of the literature. Journal of Bone & Joint Surgery - American
Volume. 1997;79(10):1545-51.
Thursday, January 07, 2010 9:22:40 AM
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