steroid metabolism, inborn errors

Preferred Label : steroid metabolism, inborn errors;

MeSH definition : Errors in metabolic processing of STEROIDS resulting from inborn genetic mutations that are inherited or acquired in utero.;

MeSH synonym : steroid metabolic diseases, inborn; inborn errors of steroid metabolism; congenital errors of steroid metabolism;

MeSH annotation : coord IM with specific steriod/metab (IM);;

Details

Origin ID

D043202;

UMLS CUI

C1257809;

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]
DO Cross reference
- steroid inherited metabolic disorder [DO Concept]
Record concept(s)
- steroid metabolism, inborn errors [MeSH concept]
Related MeSH Supplementary Concept(s)
- 17-Hydroxysteroid dehydrogenase deficiency [MeSH Supplementary Concept]
- bile acid synthesis defect, congenital, 1 [MeSH Supplementary Concept]
- bile acid synthesis defect, congenital, 2 [MeSH Supplementary Concept]
- bile acid synthesis defect, congenital, 3 [MeSH Supplementary Concept]
- cortisone reductase deficiency [MeSH Supplementary Concept]
- familial glucocorticoid deficiency 1 [MeSH Supplementary Concept]
- hypercholanemia, familial [MeSH Supplementary Concept]
- lathosterolosis [MeSH Supplementary Concept]
- lyngstadaas syndrome [MeSH Supplementary Concept]
- pseudovaginal perineoscrotal hypospadias [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- steroids [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- steroid inherited metabolic disorder [DO Concept]

Keyword's position in hierarchy(ies) :

Main resources

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