2008 ICD-9-CM Diagnosis 757.* : Congenital anomalies of the integument

Free ICD-9-CM Diagnosis Codes > 2008 > Congential Anomalies 740-759 > Congenital anomalies of the integument 757.* > 
2008 ICD-9-CM Diagnosis Code 757 Congenital anomalies of the integument
structural abnormalities of the skin that exist at, and usually before, birth regardless of their causation.
2008 ICD-9-CM Diagnosis Code 757.0Hereditary edema of legs
2008 ICD-9-CM Diagnosis Code 757.1Ichthyosis congenita
skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis that exist at, and usually before, birth regardless of their causation; most ichthyoses are genetically determined.
2008 ICD-9-CM Diagnosis Code 757.2Dermatoglyphic anomalies
2008 ICD-9-CM Diagnosis Code 757.3 Other specified congenital anomalies of skin
2008 ICD-9-CM Diagnosis Code 757.31Congenital ectodermal dysplasia
2008 ICD-9-CM Diagnosis Code 757.32Vascular hamartomas
A capillary hemangioma that may regress spontaneously. It occurs in infants and children.
2008 ICD-9-CM Diagnosis Code 757.33Congenital pigmentary anomalies of skin
most common form of mastocytosis, characterized by multiple persistant small reddish brown hyperpigmented pruritic macules and papules.
The most frequent form of cutaneous mastocytosis. In children, the lesions tend to be papular, and are characterized by aggregates of elongated or spindle-shaped mast cells which fill the papillary dermis and extend into the reticular dermis. In adults, the lesions tend to have fewer mast cells compared to those in children. The lesions are located most commonly on the trunk, but they can be seen on the extremities, head and neck. (WHO, 2001) -- 2003
rare pigmentary atrophic autosomal recessive disease manifested as an extreme photosensitivity to ultraviolet light as the result of a deficiency in the enzyme that permits excisional repair of utraviolet damaged DNA.
A genetic condition characterized by a sensitivity to all sources of ultraviolet radiation.
An inherited skin disorder characterized by photosensitivity with severe sunburn in infancy, the development of numerous pigmented spots resembling freckles, larger atrophic lesions associated with telangiectasis, and multiple solar keratoses. Transmitted in an autosomal recessive manner, xeroderma pigmentosa involves a defect in nucleotide excision repair (NER), leading to deficient repair of DNA damaged by UV radiation and chromosome breakage. Individuals with this disease develop multiple malignant cutaneous neoplasms at an early age and may suffer from severe ophthalmic and neurologic abnormalities.
2008 ICD-9-CM Diagnosis Code 757.39Other specified congenital anomalies of skin
inherited chronic noninflammatory skin disease manifested by vesicles, large bullae (blisters), and skin erosions which often result from trauma.
2008 ICD-9-CM Diagnosis Code 757.4Specified congenital anomalies of hair
2008 ICD-9-CM Diagnosis Code 757.5Specified congenital anomalies of nails
2008 ICD-9-CM Diagnosis Code 757.6Specified congenital anomalies of breast
2008 ICD-9-CM Diagnosis Code 757.8Other specified congenital anomalies of the integument
2008 ICD-9-CM Diagnosis Code 757.9Unspecified congenital anomaly of the integument
structural abnormalities of the skin that exist at, and usually before, birth regardless of their causation.
 756.*
758.* 