MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: syndromic disease (MONDO:0002254)
Parent Node: thyroid gland disease (MONDO:0003240)
..Starting node ..euthyroid sick syndrome ()
Child Nodes:
Sister Nodes:
..atrophy of thyroid ()
..C-cell hyperplasia ()
..congenital thyroid malformation without hypothyroidism ()
..euthyroid sick syndrome ()
..goiter (disease) ()
..hyperthyroidism ()
..hyperthyroxinemia ()
..hypothyroidism ()
..inherited thyroid metabolism disease ()
..thyrocalcitonin secretion disease ()
..thyroid malformation ()
..thyroid tumor ()
..thyroiditis (disease) ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6755
Name:	euthyroid sick syndrome
Definition:	Abnormal thyroid function tests, low triiodothyronine with elevated reverse triiodothyronine, in the setting of non-thyroidal illness.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	euthyroid sick syndrome; sick euthyroid syndrome; sick-euthyroid syndrome
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal