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Standards Ontologies Notations
congenital hypothyroidism

Summary
Definition
A hypothyroidism that is present at birth.
Super Class
hypothyroidism physical disorder
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 - 22 of 22 in total
Gene ID Gene Symbol Description Source
53905 DUOX1 dual oxidase 1
115111 SLC26A7 solute carrier family 26 member 7
Displaying entries 11 - 17 of 17 in total
Gene ID Gene Symbol Description Source
19017 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha
21819 Tg thyroglobulin
22018 Tpo thyroid peroxidase
22045 Trhr thyrotropin releasing hormone receptor
22095 Tshr thyroid stimulating hormone receptor
99439 Duox1 dual oxidase 1
380684 Nefh neurofilament, heavy polypeptide
Displaying entries 11 - 13 of 13 in total
Gene ID Gene Symbol Description Source
114613 Slc5a5 solute carrier family 5 member 5
266807 Duox1 dual oxidase 1
641434 Atp5pd ATP synthase peripheral stalk subunit d
Displaying all 5 entries
Gene ID Gene Symbol Description Source
32974 Zw Zwischenferment
33477 Duox Dual oxidase
43136 kumpel kin of rumpel
43826 Actbeta Activin-beta
326229 CG32669 uncharacterized protein
Displaying all 3 entries
Gene ID Gene Symbol Description Source
171608 bli-3 Dual oxidase 1
178046 gspd-1 Glucose-6-phosphate 1-dehydrogenase
186188 duox-2 NAD(P)H oxidase (H2O2-forming)
Displaying 1 entry
Gene ID Gene Symbol Description Source
855480 ZWF1 glucose-6-phosphate dehydrogenase
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024