8p11.2 deletion (Q101715): Difference between revisions
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A síndrome de deleção 8p11.2 é uma síndrome de gene contíguo caracterizada pela associação de esferocitose congênita, características dismórficas, retardo de crescimento e hipogonadismo hipogonadotrópico. | |||
| description / en | description / en | ||
8p11.2 deletion syndrome is a contiguous gene syndrome characterised by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism. | |||
Revision as of 18:33, 16 August 2026
8p11.2 deletion syndrome is a contiguous gene syndrome characterised by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1782338750 |
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| English | 8p11.2 deletion |
8p11.2 deletion syndrome is a contiguous gene syndrome characterised by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism. |
