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Syndromic recessive X-linked ichthyosis (disorder)
Syndromic recessive X-linked ichthyosis
Syndromic X-linked ichthyosis
Refers to cases of recessive X-linked ichthyosis (RXLI) that are associated with extracutaneous manifestations as part of a syndrome. It affects almost exclusively males. Cutaneous manifestations include hyperkeratosis and scaling of the skin. Non cutaneous manifestations may be corneal opacity, late puberty, cryptorchidism and a higher frequency of testicular cancer. Manifestations due to contiguous gene syndrome include neurological abnormalities such as epilepsy and hyposmia, intellectual deficit and/or short stature. Transmission is X-linked recessive.
X-gebonden recessieve ichthyosis
Id717041008
StatusPrimitive
Associated morphologyHyperkeratosis
Finding siteEntire skin
OccurrenceCongenital
Pathological processPathological developmental process
Has interpretationAbnormal
InterpretsKeratinization
ICD-10 complex map reference set
TargetQ80.1
RuleTRUE
AdviceALWAYS Q80.1
CorrelationSNOMED CT source code to target map code correlation not specified