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

4 entries on 1 page. Showing entries 1 - 4.
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Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000254048 Patient diagnoses as congenital hypothyroidism by newborn screening. Thyroid agenesis diagnosed by ultrasonography. Congenital hypothyroidism Congenital hypothyroidism by athyrosis Isolated (sporadic) 02y11m 00y02m 00y02m - - Miguel Angel Alcántara-Ortigoza 00358834
0000254049 Congenital hypothyroidism due to thyroid ectopy diagnosed by scintigraphy. Congenital hypothyroidism Congenital hypothyroidism by thyroid ectopy Isolated (sporadic) 00y11m 00y01m 00y01m - - Miguel Angel Alcántara-Ortigoza 00358835
0000254050 Congenital hypothyroidism due to thyroid ectopy diagnosed by newborn screening and scintigraphy. Congenital hypothyroidism Congenital hypothyroidism by thyroid ectopy Isolated (sporadic) 08y01m 00y01m - - - Miguel Angel Alcántara-Ortigoza 00358836
0000254051 Congenital hypothyroidism diagnosed by newborn screening. Thyroid agenesis diagnosed by ultrasonography. Pending evaluation of thyroglobulin levels (not available at this time). Congenital hypothyroidism Congenital hypothyroidism by thyroid agenesis Isolated (sporadic) 02y06m 00y01m - - - Miguel Angel Alcántara-Ortigoza 00358837
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