About: biotin deficiency

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: biotin deficiency Goto Sponge NotDistinct Permalink

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

nutritional deficiency disease that is characterized by thinning of the hair (often with loss of hair color), and red scaly rash around the eyes, nose, and mouth

Attributes	Values
rdf:type	Item
description	Krankheit (de) хвороба (uk) nutritional deficiency disease that is characterized by thinning of the hair (often with loss of hair color), and red scaly rash around the eyes, nose, and mouth (en) carence en vitamine B8 (fr)
exact match	wds:Q10264745-8FF3B8CC-54E3-4E35-AFFA-26EBD1B4AEFD wds:Q10264745-F5F4F24F-E656-4130-998B-C34C5F89887F
exact match	http://purl.obolibrary.org/obo/DOID_0050810 http://identifiers.org/doid/DOID:0050810
health specialty	wds:Q10264745-F2E25E4B-D905-4E1C-9A9D-07C82AA39254
ICD-10	wds:q10264745-F76992F3-50AE-4410-BA17-D04FDDF183D8
Mondo ID	wds:Q10264745-888CADED-7EAF-45B4-BCE1-3ECDA2AC8748
Disease Ontology ID	wds:Q10264745-3511753F-8040-446B-ACE8-C85ADB609564
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0000461
Disease Ontology ID	http://purl.obolibrary.org/obo/DOID_DOID:0050810
health specialty	endocrinology
ICD-10	E53.8
Mondo ID	MONDO_0000461
Disease Ontology ID	DOID:0050810
rdfs:label	biotin deficiency (en) deficiência de biotina (pt) déficit en biotine (fr)
skos:prefLabel	biotin deficiency (en) deficiência de biotina (pt) déficit en biotine (fr)
name	biotin deficiency (en) deficiência de biotina (pt) déficit en biotine (fr)
instance of	wds:Q10264745-37EFEEFF-D271-4D63-A162-BE85F469DA42
instance of	class of disease
subclass of	wds:Q10264745-6383F6E4-DF0E-48A5-A90C-178773B29748 wds:Q10264745-F269F825-3077-41A5-8CEC-13A147122588 wds:Q10264745-ea6a10c0-45d5-3a85-ae42-cb54d04e0586
subclass of	disease vitamin deficiency nutritional deficiency disease
eMedicine ID	wds:q10264745-728D0E92-6CB5-4001-ACD0-6016E8A54E85
eMedicine ID	984803
Medical Dictionary...ory Activities ID	wds:Q10264745-4DB2875E-8A96-4943-AEFD-5CDD31574F1F
ICD-9 ID	wds:q10264745-814B4777-A061-4810-BFF5-E10EAB72AFA5
Medical Dictionary...ory Activities ID	http://purl.bioontology.org/ontology/MDRFRE/10061580
Medical Dictionary...ory Activities ID	10061580
ICD-9 ID	266.2
skos:altLabel	B7 deficiency (en)
OpenAlex ID	wds:Q10264745-8925C052-0F4F-4561-9D22-5D8AC1878123
MeSH descriptor ID	wds:Q10264745-24A2F4F9-3D6E-40FE-AD9F-CB9481A6BA17 wds:Q10264745-f85f14b3-4566-49ff-05a2-4d5ae44a448e
on focus list of Wikimedia project	wds:Q10264745-F5BFCDDF-E332-46AF-AEC7-F041E999EAC4
Microsoft Academic ID	wds:Q10264745-FF8F52FC-ED5D-4C5E-9E7B-0455C4E37748
ICD-11 ID (MMS)	wds:Q10264745-4BD734A1-9071-4502-8DB0-FEBD2C96BAAA
ICD-11 (foundation)	wds:Q10264745-A81DF4ED-041A-4890-88CE-1999F31E40EA
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C531633
Microsoft Academic ID	https://makg.org/entity/2776294945
OpenAlex ID	C2776294945
MeSH descriptor ID	C531633
on focus list of Wikimedia project	WikiProject Medicine
Microsoft Academic ID	2776294945
ICD-11 ID (MMS)	5B5G
ICD-11 (foundation)	1726732000
WikiProjectMed ID	wds:Q10264745-F87B95D9-459C-43A3-A369-BD514FE432BB
WikiProjectMed ID	Biotin deficiency
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q10264745 Biotin deficiency https://pt.wikipedia.org/wiki/Defici%C3%AAncia_de_biotina
is main subject of	Jurkat cells respond to biotin deficiency with increased nuclear translocation of NF-kappaB, mediating cell survival Marginal biotin deficiency during normal pregnancy Experimental study of fatigue provoked by biotin deficiency in mice 3-Hydroxypropionic acid and methylcitric acid are not reliable indicators of marginal biotin deficiency in humans Interruption of the adipose conversion of 3T3 cells by biotin deficiency: differentiation without triglyceride accumulation Marginal biotin deficiency is teratogenic BIOTIN DEFICIENCY AND THE FATTY ACIDS OF CERTAIN BIOTIN-REQUIRING BACTERIA Biotin deficiency decreases ornithine transcarbamylase activity and mRNA in rat liver Biotin deficiency induces changes in subpopulations of spleen lymphocytes in mice Biotin deficiency: an unusual complication of parenteral alimentation Increased urinary excretion of 3-hydroxyisovaleric acid and decreased urinary excretion of biotin are sensitive early indicators of decreased biotin status in experimental biotin deficiency Marginal biotin deficiency is teratogenic in ICR mice Marginal biotin deficiency is common in normal human pregnancy and is highly teratogenic in mice Effects of biotin deficiency on embryonic development in mice Teratogenic effects of avidin-induced biotin deficiency in mice Regulation of intestinal biotin transport in the rat: effect of biotin deficiency and supplementation Seborrheic dermatitis of infants and Leiners's disease: a biotin deficiency Biotin deficiency in an infant fed with amino acid formula Indicators of marginal biotin deficiency and repletion in humans: validation of 3-hydroxyisovaleric acid excretion and a leucine challenge Lymphocyte propionyl-CoA carboxylase is an early and sensitive indicator of biotin deficiency in rats, but urinary excretion of 3-hydroxypropionic acid is not Urinary excretion of 3-hydroxyisovaleryl carnitine is an early and sensitive indicator of marginal biotin deficiency in humans Marginal biotin deficiency can be induced experimentally in humans using a cost-effective outpatient design Human Biotin Deficiency Lymphocyte propionyl-CoA carboxylase and accumulation of odd-chain fatty acid in plasma and erythrocytes are useful indicators of marginal biotin deficiency small star, filled Clinical biotin deficiency (egg white injury); report of a case with some remarks on serum cholesterol Effects of biotin deficiency on pancreatic islet morphology, insulin sensitivity and glucose homeostasis. Marginal biotin deficiency is teratogenic in mice and perhaps humans: a review of biotin deficiency during human pregnancy and effects of biotin deficiency on gene expression and enzyme activities in mouse dam and fetus Activities of pyruvate carboxylase and propionyl CoA carboxylase in rat tissues during biotin deficiency and restoration of the activities after biotin administration. OBSERVATIONS ON THE FINE STRUCTURE OF SACCHAROMYCES CEREVISIAE AS AFFECTED BY BIOTIN DEFICIENCY Biotin deficiency as the causative agent of induced cryptorchidism in albino rats Biotin transport in primary culture of astrocytes: effect of biotin deficiency Biotin deficiency in protein-energy malnutrition: implications for nutritional homeostasis and individuality Some Biochemical Observations on Biotin Deficiency in the Rat as a Model for Human Pyruvate Carboxylase Deficiency Effect of biotin deficiency on follicular melanocytes of mice Marginal maternal biotin deficiency in CD-1 mice reduces fetal mass of biotin-dependent carboxylases Biotin deficiency enhances the inflammatory response of human dendritic cells.

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software