skin abnormalities

Preferred Label : skin abnormalities;

MeSH definition : Congenital structural abnormalities of the skin.;

MeSH synonym : abnormalities, skin; abnormality, skin; skin abnormality;

MeSH annotation : for congen struct abnorm only; GEN or unspecified; prefer specifics; DF: SKIN ABNORM; for congen struct abnorm only; GEN or unspecified; prefer specifics; for congenital structural abnormalities only; general or unspecified; prefer specifics;

Details

Origin ID

D012868;

UMLS CUI

C0037268;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Abnormality of the skin [HPO term]
- Congenital Skin Disorder [NCIt concept]
- Congenital anomaly of skin [ICPC-3 diagnosis]
- Congenital anomaly of skin (disorder) [SNOMED CT concept]
- Other congenital malformations of skin [ICD-10 category (who)]
- Skin malformation [MedDRA Preferred Term]
- Structural developmental anomalies of the skin [Bloc CIM-11]
- congenital anomaly of skin, nos [SNOMED Notion]
- congenital skin anomaly other [ICPC-2 Rubric]
HPO term
- Abnormality of the skin [HPO term]
Mapping VCM exact
- deformity [VCM modifier]
MeSH Descriptor(s) used for indexing
- skin [MeSH Descriptor]
Record concept(s)
- skin abnormalities [MeSH concept]
Related MeSH Supplementary Concept(s)
- Brittle cornea syndrome 1 [MeSH Supplementary Concept]
- Hypohidrosis with Abnormal Palmar Dermal Ridges [MeSH Supplementary Concept]
- Ichthyosis-Mental retardation syndrome with large keratohyalin granules in the skin [MeSH Supplementary Concept]
- Midline brainstem cleft [MeSH Supplementary Concept]
- Skin-Hair-Eye Pigmentation, Variation In, 10 [MeSH Supplementary Concept]
- Skin-Hair-Eye Pigmentation, Variation In, 11 [MeSH Supplementary Concept]
- Skin-Hair-Eye Pigmentation, Variation In, 4 [MeSH Supplementary Concept]
- Skin-Hair-Eye Pigmentation, Variation In, 5 [MeSH Supplementary Concept]
- Skin-Hair-Eye Pigmentation, Variation In, 6 [MeSH Supplementary Concept]
- Skin-Hair-Eye Pigmentation, Variation In, 7 [MeSH Supplementary Concept]
- Skin-Hair-Eye Pigmentation, Variation In, 8 [MeSH Supplementary Concept]
- Skin-Hair-Eye Pigmentation, Variation In, 9 [MeSH Supplementary Concept]
- arthropathy, erosive [MeSH Supplementary Concept]
- barber say syndrome [MeSH Supplementary Concept]
- blepharophimosis syndrome type 1 [MeSH Supplementary Concept]
- blepharophimosis syndrome type 2 [MeSH Supplementary Concept]
- blepharophimosis with ptosis, syndactyly, and short stature [MeSH Supplementary Concept]
- blepharophimosis, ptosis, and epicanthus inversus [MeSH Supplementary Concept]
- book syndrome [MeSH Supplementary Concept]
- comedones, familial dyskeratotic [MeSH Supplementary Concept]
- cutis gyrata syndrome of beare and stevenson [MeSH Supplementary Concept]
- dermal ridges, nelson syndrome [MeSH Supplementary Concept]
- dermal ridges, patternless [MeSH Supplementary Concept]
- dermoodontodysplasia [MeSH Supplementary Concept]
- dyskeratosis, hereditary benign intraepithelial [MeSH Supplementary Concept]
- epithelial squamous dysplasia, keratinizing desquamative, of urinary tract [MeSH Supplementary Concept]
- familial popliteal pterygium syndrome [MeSH Supplementary Concept]
- hairy palms and soles [MeSH Supplementary Concept]
- hemangiomatosis, cutaneous, with associated features [MeSH Supplementary Concept]
- hyperkeratotic cutaneous Capillary-Venous malformations associated with cerebral capillary malformations [MeSH Supplementary Concept]
- keratosis linearis with ichthyosis congenita and sclerosing keratoderma [MeSH Supplementary Concept]
- michelin tire baby syndrome [MeSH Supplementary Concept]
- microphthalmia, syndromic 7 [MeSH Supplementary Concept]
- multiple pterygium syndrome [MeSH Supplementary Concept]
- oculocerebrocutaneous syndrome [MeSH Supplementary Concept]
- poikiloderma with neutropenia [MeSH Supplementary Concept]
- poikiloderma, hereditary sclerosing [MeSH Supplementary Concept]
- pterygium colli, isolated [MeSH Supplementary Concept]
- ridges-off-the-end syndrome [MeSH Supplementary Concept]
- tight skin contracture syndrome, lethal [MeSH Supplementary Concept]
- urban schosser spohn syndrome [MeSH Supplementary Concept]
- vascular hyalinosis [MeSH Supplementary Concept]
- winter shortland temple syndrome [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- skin [MeSH Descriptor]
See also inter- (CISMeF)
- Abnormality of the skin [HPO term]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Abnormality of the skin [HPO term]
- Congenital Skin Disorder [NCIt concept]
- Congenital anomaly of skin (disorder) [SNOMED CT concept]
- Congenital malformation of skin, unspecified [ICD-10 Sub-category]
- Congenital malformation of skin, unspecified [ICD-10 Sub-category (who)]
- Congenital skin disorder [MedDRA Preferred Term]
- SKIN MALFORMATION [WHO-ART Preferred Term]
- Skin malformation [MedDRA Preferred Term]
- congenital anomaly of integument, nos [SNOMED Notion]
- congenital anomaly of skin, nos [SNOMED Notion]
- congenital skin disorder [Disease (Nov.)]
Validated automatic mappings to BTNT
- congenital skin disorder [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients