congenital hypothyroidism

Summary
Definition
A hypothyroidism that is present at birth.
Super Class
hypothyroidism physical disorder
External Links
Disease Ontology
DOID:0050328
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 41 - 50 of 58 in total
Gene ID Gene Symbol Description Source
5743 PTGS2 prostaglandin-endoperoxide synthase 2
6515 SLC2A3 solute carrier family 2 member 3
6715 SRD5A1 steroid 5 alpha-reductase 1
8879 SGPL1 sphingosine-1-phosphate lyase 1
8985 PLOD3 procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
9415 FADS2 fatty acid desaturase 2
9526 MPDU1 mannose-P-dolichol utilization defect 1
10020 GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
10891 PPARGC1A PPARG coactivator 1 alpha
23583 SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
Displaying all 3 entries
Gene ID Gene Symbol Description Source
14380 G6pd2 glucose-6-phosphate dehydrogenase 2
14381 G6pdx glucose-6-phosphate dehydrogenase X-linked
19017 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha
Displaying all 2 entries
Gene ID Gene Symbol Description Source
24377 G6pd glucose-6-phosphate dehydrogenase
83516 Ppargc1a PPARG coactivator 1 alpha
Displaying 1 entry
Gene ID Gene Symbol Description Source
32974 Zw Zwischenferment
Displaying 1 entry
Gene ID Gene Symbol Description Source
178046 gspd-1 Glucose-6-phosphate 1-dehydrogenase
Displaying 1 entry
Gene ID Gene Symbol Description Source
855480 ZWF1 glucose-6-phosphate dehydrogenase

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Last updated: August 19, 2024