ichthyosis - CISMeF

Preferred Label : ichthyosis;

MeSH definition : Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome.;

MeSH synonym : ichthyoses;

Related MeSH term : xeroderma; Xerodermas;

MeSH annotation : GEN or unspecified; prefer specifics; unspecified dryness of skin is indexed under SKIN DISEASES, not here; general or unspecified; prefer specifics; unspecified dryness of skin is indexed under SKIN DISEASES, not here;

Wikipedia link : https://en.wikipedia.org/wiki/Ichthyosis;

Details

Origin ID

D007057;

UMLS CUI

C0020757;

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)
- Congenital ichthyosis of skin (disorder) [SNOMED CT concept]
- Dry skin disorder [ICD-11 Category]
- Other manifestations of vitamin A deficiency [ICD-10 Sub-category]
- XERODERMA [WHO-ART Included Term]
- Xeroderma [PASCAL descriptor]
- Xeroderma [MedDRA Preferred Term]
- Xeroderma [NCIt concept]
- Xeroderma (disorder) [SNOMED CT concept]
- congenital ichthyosis of skin, nos [SNOMED Notion]
- skin disease other [ICPC-2 Rubric]
- xeroderma, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- ICHTHYOSIS [WHO-ART Included Term]
- Ichthyoses [MedDRA High Level Term]
- Ichthyoses [ICD-11 Category]
- Ichthyosis [HPO term]
- Ichthyosis [PASCAL descriptor]
- Ichthyosis [HPO term]
- Ichthyosis [MedDRA Preferred Term]
- Ichthyosis [NCIt concept]
- Ichthyosis [ORDO Disease]
- Ichthyosis (disorder) [SNOMED CT concept]
- Skin change ichthyosiform [MedDRA LLT]
- ichthyosis [Disease (Nov.)]
- ichthyosis [DO Concept]
DO Cross reference
- ichthyosis [DO Concept]
HPO term
- Ichthyosis [HPO term]
Manual NTBT mappings (CISMeF)
- Al-Gazali-Dattani syndrome [ORDO Disease]
- Congenital cataract-ichthyosis syndrome [ORDO Disease]
- Congenital ichthyosis-microcephalus-tetraplegia syndrome [ORDO Disease]
- Epidermal disease [ORDO Disease]
- Fanconi syndrome-ichthyosis-dysmorphism syndrome [ORDO Disease]
- IBIDS syndrome [ORDO Disease]
- Ichthyosis associated with a cornified cell envelope and epidermal lipid metabolism anomaly [ORDO Disease]
- Ichthyosis associated with a nucleotide excision repair anomaly [ORDO Disease]
- Ichthyosis associated with a peroxisomal disease [ORDO Disease]
- Ichthyosis associated with a protein catabolism anomaly [ORDO Disease]
- Ichthyosis-cheek-eyebrow syndrome [ORDO Disease]
- Ichthyosis-hypotrichosis syndrome [ORDO Disease]
- Ichthyosis-oral and digital anomalies syndrome [ORDO Disease]
- Ichthyosis-prematurity syndrome [ORDO Disease]
- Keratoderma hereditarium mutilans with ichthyosis [ORDO Disease]
- MEDNIK syndrome [ORDO Disease]
- Neonatal ichthyosis-sclerosing cholangitis syndrome [ORDO Disease]
- Osteosclerosis-ichthyosis-premature ovarian failure syndrome [ORDO Disease]
- Peeling skin syndrome [ORDO Disease]
- Restrictive dermopathy [ORDO Disease]
ORDO relation(s)
- Ichthyosis [ORDO Disease]
Record concept(s)
- ichthyosis [MeSH concept]
- xeroderma [MeSH concept]
Related MeSH Supplementary Concept(s)
- HID syndrome [MeSH Supplementary Concept]
- Ichthyosis-Mental retardation syndrome with large keratohyalin granules in the skin [MeSH Supplementary Concept]
- Trichodysplasia-Xeroderma [MeSH Supplementary Concept]
- acquired ichthyosis [MeSH Supplementary Concept]
- camptodactyly-ichthyosis syndrome [MeSH Supplementary Concept]
- cataract and congenital ichthyosis [MeSH Supplementary Concept]
- deal barratt dillon syndrome [MeSH Supplementary Concept]
- dykes markes harper syndrome [MeSH Supplementary Concept]
- erythrokeratoderma, reticular [MeSH Supplementary Concept]
- grover's disease [MeSH Supplementary Concept]
- ichthyosis cheek eyebrow syndrome [MeSH Supplementary Concept]
- ichthyosis exfoliativa [MeSH Supplementary Concept]
- ichthyosis follicularis atrichia photophobia syndrome [MeSH Supplementary Concept]
- ichthyosis hystrix gravior [MeSH Supplementary Concept]
- ichthyosis hystrix, curth macklin type [MeSH Supplementary Concept]
- ichthyosis prematurity syndrome [MeSH Supplementary Concept]
- ichthyosis tapered fingers midline groove up [MeSH Supplementary Concept]
- ichthyosis with hypotrichosis, autosomal recessive [MeSH Supplementary Concept]
- ichthyosis, X-Linked, complicated [MeSH Supplementary Concept]
- ichthyosis, congenital, autosomal recessive, Ichthyin-Related [MeSH Supplementary Concept]
- ichthyosis, congenital, with trichothiodystrophy [MeSH Supplementary Concept]
- ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis [MeSH Supplementary Concept]
- ichthyosis, mental retardation, dwarfism, and renal impairment [MeSH Supplementary Concept]
- ichthyosis, nonlamellar and nonerythrodermic, congenital, autosomal recessive [MeSH Supplementary Concept]
- ichthyosis, split hairs, and amino aciduria [MeSH Supplementary Concept]
- jagell holmgren hofer syndrome [MeSH Supplementary Concept]
- keratitis, ichthyosis, and deafness (KID) syndrome [MeSH Supplementary Concept]
- keratosis follicularis spinulosa decalvans, X-Linked [MeSH Supplementary Concept]
- koone rizzo elias syndrome [MeSH Supplementary Concept]
- neu laxova syndrome [MeSH Supplementary Concept]
- osteosclerosis with ichthyosis and fractures [MeSH Supplementary Concept]
- rud syndrome [MeSH Supplementary Concept]
- ruzicka goerz anton syndrome [MeSH Supplementary Concept]
- sammartino de crecchio syndrome [MeSH Supplementary Concept]
- stormorken syndrome [MeSH Supplementary Concept]
- zunich neuroectodermal syndrome [MeSH Supplementary Concept]
See also (automatic)
- XERODERMA [WHO-ART Included Term]
- Xeroderma [MedDRA Preferred Term]
- xeroderma, nos [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ICHTHYOSIS [WHO-ART Included Term]
- Ichthyoses [MedDRA High Level Term]
- Ichthyosis [MedDRA Preferred Term]
- Ichthyosis [ORDO Disease]
- Ichthyosis [HPO term]
- Ichthyosis [HPO term]
- Ichthyosis [PASCAL descriptor]
- Ichthyosis [NCIt concept]
- Ichthyosis (disorder) [SNOMED CT concept]
- Skin change ichthyosiform [MedDRA LLT]
- ichthyosis [DO Concept]
- ichthyosis [Disease (Nov.)]
Validated automatic mappings to NTBT
- xerosis [Disease (Nov.)]

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