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 21 - 30 of 58 in total
Gene ID Gene Symbol Description Source
2876 GPX1 glutathione peroxidase 1
3283 HSD3B1 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1
3293 HSD17B3 hydroxysteroid 17-beta dehydrogenase 3
3633 INPP5B inositol polyphosphate-5-phosphatase B
3897 L1CAM L1 cell adhesion molecule
3958 LGALS3 galectin 3
3990 LIPC lipase C, hepatic type
4153 MBL2 mannose binding lectin 2
4684 NCAM1 neural cell adhesion molecule 1
5167 ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 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