Disease #01729 (CHNG2 (hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia, type 2 (CHNG2)), OMIM:218700)

Official abbreviation CHNG2
Name hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia, type 2 (CHNG2)
OMIM ID 218700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene PAX8
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-03-16 10:43:15 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00358834 HC-266 PubMed: Alcántara-Ortigoza 2021 - F no Mexico Mexican - - yes Thyroid hormone supplementation CHNG2 Patient diagnoses as congenital hypothyroidism by newborn screening. Thyroid agenesis diagnosed by ultrasonography. FOXE1, NKX2-5, TSHR FOXE1 1 1 Miguel Angel Alcántara-Ortigoza
00358835 HC-215 PubMed: Alcántara-Ortigoza 2021 - F no Mexico Mexican - - yes Thyroid hormone supplementation CHNG2 Congenital hypothyroidism due to thyroid ectopy diagnosed by scintigraphy. FOXE1 FOXE1 1 1 Miguel Angel Alcántara-Ortigoza
00358836 HC-321 PubMed: Alcántara-Ortigoza 2021 - M no Mexico Mexican - 1 yes Thyroid hormone supplementation CHNG2 Congenital hypothyroidism due to thyroid ectopy diagnosed by newborn screening and scintigraphy. NKX2-5 NKX2-5 1 1 Miguel Angel Alcántara-Ortigoza
00358837 HC-324 PubMed: Alcántara-Ortigoza 2021 - F no Mexico Mexican - - yes Thyroid hormone supplementation CHNG2 Congenital hypothyroidism diagnosed by newborn screening. Thyroid agenesis diagnosed by ultrasonography. Pending evaluation of thyroglobulin levels (not available at this time). TSHR TSHR 2 1 Miguel Angel Alcántara-Ortigoza
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