- X linked ichthyosis
- 엑스연관어린선
English-Korean animal medical dictionary. 2013.
X linked ichthyosis
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X-linked ichthyosis — Infobox Disease Name = X linked ichthyosis Caption = DiseasesDB = 29136 ICD10 = ICD10|Q|80|1|q|80 ICD9 = ICD9|757.1 ICDO = OMIM = 308100 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 191 MeshID = D016114 X linked ichthyosis (XLI) is a skin… … Wikipedia
X-linked ichthyosis — a chronic, X linked ichthyosis caused by deficiency of the microsomal enzyme steryl sulfatase as a result of mutation in the STS gene (locus: Xp22.32); it may be present at birth or appear in early infancy. It is characterized by prominent,… … Medical dictionary
Ichthyosis — Classification and external resources Ichthyosis is recognized by rough, scaly skin exhibited by patients. ICD 10 Q … Wikipedia
Ichthyosis vulgaris — Classification and external resources Ichthyosis vulgaris #1 (top left) ICD 10 Q … Wikipedia
Ichthyosis — Dry, rectangular scales on the skin. Like fish scales. From the Greek ichthys meaning fish. Ichthyosis is not one but rather a group of skin disorders characterized by noninflammatory scaling of the skin. Many different metaphors have been used… … Medical dictionary
Lamellar ichthyosis — Ichthyosis lamellaris Classification and external resources ICD 10 Q80.2 OMIM 242300 DiseasesDB … Wikipedia
Ichthyosis vulgaris — A genetic skin disease that is inherited as an autosomal (nonsex linked) trait and is characterized by scaly (fishlike) areas of skin. The first scaly skin problems usually appear after 3 months of age. The palms and soles are often affected.… … Medical dictionary
X-linked lymphoproliferative disease — Classification and external resources ICD 10 D82.3 OMIM 308240 300635 … Wikipedia
X-linked adrenal hypoplasia congenita — Classification and external resources OMIM 300200 DiseasesDB 32988 X linked adrenal hypoplasia congenita is a genetic dis … Wikipedia
X-linked congenital stationary night blindness — Classification and external resources Malfunction in transmission from the photoreceptors in the outer nuclear layer to bipolar cells in the inner nuclear layer underlies CSNB. ICD … Wikipedia
Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome — Classification and external resources OMIM 609528 Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome (also known as CEDNIK syndrome ) is a cutaneous condition caused by mutation in the SNAP29 gene.[ … Wikipedia
