About: skin abnormality

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

human disease

Attributes	Values
rdf:type	Item
description	human disease (en) хвороба людини (uk) مرض يصيب الإنسان (ar)
exact match	wds:Q19000678-1E278881-77D5-4C2E-84BB-4834A7F97C70 wds:Q19000678-BBB54393-EB36-4FF2-A1B5-259E5DE2BC5A
health specialty	wds:Q19000678-C8EA0FBD-745A-4B42-B6D3-C4693E7695BD
Disease Ontology ID	wds:Q19000678-E916D52D-2AD8-4F85-9096-C65255B504DD
health specialty	dermatology
rdfs:label	malformations cutanées (fr) skin abnormality (en) ādas anomālijas (lv)
skos:prefLabel	malformations cutanées (fr) skin abnormality (en) ādas anomālijas (lv)
name	malformations cutanées (fr) skin abnormality (en) ādas anomālijas (lv)
subclass of	wds:Q19000678-a4a737b8-4441-5e2b-5c5f-e7fcef0ebd39 wds:Q19000678-cd21b2ec-4dc8-dbff-567c-efbd80f28ab3
subclass of	skin disease congenital physical abnormality
ICD-9 ID	wds:Q19000678-115B93B6-0245-4BC3-BC42-4F4CAADC1D15 wds:Q19000678-18BB5691-246F-4EDE-A5D5-21F130BD375E
ICD-9 ID	757 757.9
skos:altLabel	obsolete skin abnormality (en) skin abnormalities (en)
National Library of Latvia ID	wds:Q19000678-c2c48ec3-4047-c04a-165c-a6121a0d210e
UMLS CUI	wds:Q19000678-81947A7B-E8EC-441F-AD27-5A4AD2F32A41
MeSH descriptor ID	wds:Q19000678-76542CAF-837B-4819-BACD-ED0E00B614A5
on focus list of Wikimedia project	wds:Q19000678-2D3A2BD9-4EE1-4D45-9543-321B618A5802
MeSH tree code	wds:Q19000678-9F45FCDF-27CF-4EF8-9E1C-FA76F9D27F29 wds:Q19000678-A3417624-B049-4E1A-80EB-31D0E81F0423
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D012868
MeSH tree code	http://id.nlm.nih.gov/mesh/C16.131.831 http://id.nlm.nih.gov/mesh/C17.800.804
National Library of Latvia ID	000092115
UMLS CUI	C0037268
MeSH descriptor ID	D012868
on focus list of Wikimedia project	WikiProject Medicine
MeSH tree code	C16.131.831 C17.800.804
is owl:sameAs of	skin abnormality
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q19000678
is main subject of	Congenital Localized Absence of Skin and Associated Abnormalities Resembling Epidermolysis Bullosa Knuckle pads, leukonychia, deafness, and keratosis palmoplantaris: report of a family alpha1-Antitrypsin Deficiency and Skin Abnormalities A NEW SYNDROME COMBINING PTERYGIUM COLLI WITH DEVELOPMENTAL ANOMALIES OF THE EYELIDS AND LYMPHATICS OF THE LOWER EXTREMITIES The expression of the gene asebia in the laboratory mouse: I. Epidermis and dermis Repeated epilation: a genetic epidermal syndrome in mice Undiagnosed syndrome of psychomotor retardation, low birthweight dwarfism, skeletal, dental, dermal and genital anomalies Hairy cutaneous malformations of palms and soles. A hereditary condition Human tails and pseudotails Congenital skin defects and fetus papyraceus Aplasia cutis congenita in two sibs discordant for pylori atresia Hair loss and cyst formation in hairless and rhino mutant mice Unilateral limb and skin deformities with congenital heart disease in two siblings: A lethal syndrome Congenital dermal sinuses in children; their relation to pilonidal sinuses Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects Rib-gap defect with micrognathia, malformed tracheal cartilages, and redundant skin: A new pattern of defective development Clinical aspects of congenital skin defects. I. Congenital skin defects on the head of the newborn The stiff skin syndrome Cardio-Facio-cutaneous (CFC) syndrome: Report of two patients without hyperkeratotic skin lesions Restrictive dermopathy: a disorder of fibroblasts Cardio-facio-cutaneous syndrome: three additional cases and review of the literature Costello syndrome and neurological abnormalities Beare-Stevenson cutis gyrata syndrome Lipid deficiencies, leukocytosis, brittle skin--a lethal syndrome caused by a recessive mutation, edematous (oed), in the mouse Dermoid Sinus in the Rhodesian Ridgeback Study of the normal skin and of some of its malformations, using the scansion microscope Midline cutaneous and spinal defects. Midline cutaneous abnormalities associated with occult spinal disorders Skin Blisters And Hair Loss In A Rat Mutant Called Vibrissaeless(vb) Gerodermia osteodysplastica/wrinkly skin syndrome: Report of three patients and brief review of the literature A case of dermal sinus of the nose with frontal suppuraton Seven apparently congenital non-infectious conditions of the skin of the pig, resembling congenital defects in man Palmodigital purpura as the only skin abnormality in myeloma-associated systemic amyloidosis Skin abnormality in aged fyn-/- fak+/- mice. Congenital localized absence of the skin as a manifestation of epidermolysis bullosa The François Dyscephalic Syndrome and Skin Manifestations Absence of the d triradius Hereditary fragility and hyperextensibility of the skin of cats. A defect in collagen fibrillogenesis Neurological complications in one of a sibpair with aplasia cutis congenita Ocular Manifestations of Focal Dermal Hypoplasia Syndrome Congenital Absence of Skin (Aplasia Cutis Congenita) IQ and the somatic stigmata of Turner's syndrome Dermatoleukodystrophy with neuroaxonal spheroids Cutaneous Abnormalities and their Relationship to the Underlying Tissues The Manifestations and Complications of Intraspinal Congenital Dermal Sinuses and Dermoid Cysts A case of human pseudo-tail Abnormal keratinization in the pupoid fetus () mutant mouse epidermis Congenital localized absence of skin, blistering and nail abnormalities, a new syndrome Congenital ectodermal defect with nail dystrophy and resorption of terminal phalanges Cutaneous congenital aplasia. 2 cases observed at 2 successive births Extensive congenital cutaneous aplasia of the upper extremity in the newborn. (Apropos of a case) Diagnostic and clinical significance of striae-like skin changes in the lumbosacral region Anomalies and malformation in the shells of Crassostrea virginica Curiosa paediatrica II The structure and tensile properties of the skin of tight-skin (Tsk) mutant mice An unusual case of extensive cutaneous aplasia

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