Preferred Name | Hypothyroidism, congenital, non-goitrous, 2 | |
Synonyms |
CHNG2 |
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Definitions |
(CHNG2) - A disease characterized by thyroid dysgenesis, the most frequent cause of congenital hypothyroidism, accounting for 85% of case. The thyroid gland can be completely absent (athyreosis), ectopically located and|or severely hypoplastic. Ectopic thyroid gland is the most frequent malformation, with thyroid tissue being found most often at the base of the tongue. |
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ID |
http://identifiers.org/omim/218700 |
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altLabel |
CHNG2 |
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definition |
(CHNG2) - A disease characterized by thyroid dysgenesis, the most frequent cause of congenital hypothyroidism, accounting for 85% of case. The thyroid gland can be completely absent (athyreosis), ectopically located and|or severely hypoplastic. Ectopic thyroid gland is the most frequent malformation, with thyroid tissue being found most often at the base of the tongue. |
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id |
OMIM:218700 |
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notation |
OMIM:218700 |
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prefLabel |
Hypothyroidism, congenital, non-goitrous, 2 |
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subClassOf |