2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Congential Anomalies 740-759 > Congenital Anomalies Of The Integument 757.* >  2008 ICD-9-CM Diagnosis 757.31
Congenital ectodermal dysplasia- A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita.
- 757.31 is a specific code that can be used to specify a diagnosis
- 757.31 contains 13 index entries
- View the ICD-9-CM Volume 1 757.* hierarchy
Index entries containing 757.31:- Basan's (hidrotic) ectodermal dysplasia
 757.31
Bason's (hidrotic) ectodermal dysplasia 757.31
Clouston's (hidrotic) ectodermal dysplasia 757.31
Dysplasia - see also Anomaly- ectodermal (anhidrotic) (Bason) (Clouston's) (congenital) (Feinmesser) (hereditary) (hidrotic) (Marshall) (Robinson's) 757.31
- hypohidrotic ectodermal 757.31
Ectodermal dysplasia, congenital 757.31
Feinmesser's (hidrotic) ectodermal dysplasia 757.31
Hypohidrotic ectodermal dysplasia 757.31
Marshall's (hidrotic) ectodermal dysplasia 757.31
Robinson's (hidrotic) ectodermal dysplasia 757.31
Siemens' syndrome- ectodermal dysplasia 757.31
Syndrome - see also Disease- Clouston's (hidrotic ectodermal dysplasia) 757.31
- Siemens'
- ectodermal dysplasia 757.31
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