Gonadotropin insensitivity

Gonadotropin insensitivity includes:

Luteinizing hormone insensitivity
Follicle-stimulating hormone insensitivity

See also

Gonadotropin-releasing hormone insensitivity

References

Gonadal disorder

Ovarian

Polycystic ovary syndrome
Premature ovarian failure
Hyperthecosis

Testicular

Enzymatic	5α-Reductase 2 deficiency 17β-Hydroxysteroid dehydrogenase deficiency Aromatase excess syndrome
Androgen receptor	Androgen insensitivity syndrome Mild androgen insensitivity syndrome Partial androgen insensitivity syndrome Complete androgen insensitivity syndrome Familial male-limited precocious puberty
Other	Sertoli cell-only syndrome

General

Hypogonadism
- Delayed puberty
Hypergonadism
- Precocious puberty
Hypoandrogenism
Hypoestrogenism
Hyperandrogenism
Hyperestrogenism
Postorgasmic illness syndrome
Cytochrome P450 oxidoreductase deficiency
Cytochrome b5 deficiency
Androgen-dependent condition
Aromatase deficiency
Estrogen insensitivity syndrome
Hypergonadotropic hypogonadism
Hypogonadotropic hypogonadism
Fertile eunuch syndrome
Estrogen-dependent condition
Premature thelarche
Gonadotropin insensitivity
Hypergonadotropic hypergonadism

Cell surface receptor deficiencies

G protein-coupled receptor
(including hormone)

Class A	TSHR (Congenital hypothyroidism 1) LHCGR (Luteinizing hormone insensitivity, Leydig cell hypoplasia, Male-limited precocious puberty) FSHR (Follicle-stimulating hormone insensitivity, XX gonadal dysgenesis) GnRHR (Gonadotropin-releasing hormone insensitivity) EDNRB (ABCD syndrome, Waardenburg syndrome 4a, Hirschsprung's disease 2) AVPR2 (Nephrogenic diabetes insipidus 1) PTGER2 (Aspirin-exacerbated respiratory disease)
Class B	PTH1R (Jansen's metaphyseal chondrodysplasia)
Class C	CASR (Familial hypocalciuric hypercalcemia)
Class F	FZD4 (Familial exudative vitreoretinopathy 1)

Enzyme-linked receptor
(including
growth factor)

RTK	ROR2 (Robinow syndrome) FGFR1 (Pfeiffer syndrome, KAL2 Kallmann syndrome) FGFR2 (Apert syndrome, Antley–Bixler syndrome, Pfeiffer syndrome, Crouzon syndrome, Jackson–Weiss syndrome) FGFR3 (Achondroplasia, Hypochondroplasia, Thanatophoric dysplasia, Muenke syndrome) INSR (Donohue syndrome Rabson–Mendenhall syndrome) NTRK1 (Congenital insensitivity to pain with anhidrosis) KIT (KIT Piebaldism, Gastrointestinal stromal tumor)
STPK	AMHR2 (Persistent Müllerian duct syndrome II) TGF beta receptors: Endoglin/Alk-1/SMAD4 (Hereditary hemorrhagic telangiectasia) TGFBR1/TGFBR2 (Loeys–Dietz syndrome)
GC	GUCY2D (Leber's congenital amaurosis 1)

Type I cytokine receptor: GH (Laron syndrome)
CSF2RA (Surfactant metabolism dysfunction 4)

MPL (Congenital amegakaryocytic thrombocytopenia)

TNFRSF1A (TNF receptor associated periodic syndrome)
TNFRSF13B (Selective immunoglobulin A deficiency 2)
TNFRSF5 (Hyper-IgM syndrome type 3)
TNFRSF13C (CVID4)
TNFRSF13B (CVID2)
TNFRSF6 (Autoimmune lymphoproliferative syndrome 1A)

Lipid receptor

LRP: LRP2 (Donnai–Barrow syndrome)
LRP4 (Cenani–Lenz syndactylism)
LRP5 (Worth syndrome, Familial exudative vitreoretinopathy 4, Osteopetrosis 1)

LDLR (LDLR Familial hypercholesterolemia)

Other/ungrouped

Immunoglobulin superfamily: AGM3, 6

Integrin: LAD1
Glanzmann's thrombasthenia
Junctional epidermolysis bullosa with pyloric atresia

EDAR (EDAR hypohidrotic ectodermal dysplasia)

PTCH1 (Nevoid basal-cell carcinoma syndrome)
BMPR1A (BMPR1A juvenile polyposis syndrome)
IL2RG (X-linked severe combined immunodeficiency)

See also: cell surface receptors

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.