A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait.
See also reference (FX) in Slovak
hormón uvoľňujúci gonadotropín receptor fibroblastového rastového faktora, typ 1
See also reference (FX) in English
Gonadotropin-Releasing Hormone Receptor, Fibroblast Growth Factor, Type 1
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(2) - MeSH descriptor
(1) - CiBaMed
subject heading
openseadragon
Number of the records: 1
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