Alphabetic Index · main term
Siemens' syndrome (ectodermal dysplasia)
Siemens' syndrome (ectodermal dysplasia) is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists Q82.8 for this term: Other specified congenital malformations of skin. It is a billable code. Confirm any code you find here in the Tabular List before you report it.
Code the Index gives
Other specified congenital malformations of skin
Other Index terms that lead to Q82.8
Different words, same code. 53 entries
- Abnormal, abnormality, abnormalities, palmar creases
- Acanthosis (acquired) (nigricans), benign
- Acanthosis (acquired) (nigricans), congenital
- Accessory (congenital), skin tags
- Angiomatosis
- Anomaly, anomalous (congenital) (unspecified type), dermatoglyphic
- Anomaly, anomalous (congenital) (unspecified type), pigmentation, congenital
- Anomaly, anomalous (congenital) (unspecified type), simian crease
- Bloom (-Machacek)(-Torre) syndrome
- Brugsch's syndrome
- Cutis, hyperelastica
- Cutis, verticis gyrata
Show 41 more
- Darier (-White) disease (congenital)
- Dermatolysis (exfoliativa) (congenital)
- Dermatomegaly NEC
- Disease, diseased, Naegeli's
- Dyskeratosis, congenital
- Dysplasia, ectodermal (anhidrotic) (congenital) (hereditary), hydrotic
- Elastic skin
- Elastoma (juvenile)
- Gyrate scalp
- Hailey-Hailey disease
- Hyperkeratosis, follicularis
- Hypoplasia, hypoplastic, focal dermal
- Hypoplasia, hypoplastic, skin
- Ichthyosis (congenital), palmaris and plantaris
- India rubber skin
- Keratoderma, keratodermia (congenital) (palmaris et plantaris) (symmetrical)
- Keratoma, palmaris and plantaris hereditarium
- Keratosis, follicularis
- Keratosis, follicularis, congenita
- Keratosis, follicularis, spinulosa (decalvans)
- Keratosis, palmaris et plantaris (inherited) (symmetrical)
- Keratosis, vegetans
- Lax, laxity, skin (acquired), congenital
- Lichen, congenital
- Lichen, pilaris
- Melanocytosis, neurocutaneous
- Mibelli's disease (porokeratosis)
- Naegeli's, disease
- Pachydermatocele (congenital)
- Particolored infant
- Pemphigus, benign familial (chronic)
- Pigmentation (abnormal) (anomaly), lids, congenital
- Pigmentation (abnormal) (anomaly), scrotum, congenital
- Poikiloderma, congenital
- Porokeratosis
- Pseudoxanthoma elasticum
- Rothmund (-Thomson) syndrome
- Syndrome, telangiectasic-pigmentation-cataract
- Tag (hypertrophied skin) (infected), skin, accessory (congenital)
- Tag (hypertrophied skin) (infected), skin, congenital
- Tylosis (acquired), palmaris et plantaris (congenital) (inherited)