Pages that link to "Familial male-limited precocious puberty"
Showing 50 items.
- Endocrinology (links | edit)
- 5α-Reductase 2 deficiency (links | edit)
- Androgen insensitivity syndrome (links | edit)
- Polycystic ovary syndrome (links | edit)
- Penetrance (links | edit)
- Anastrozole (links | edit)
- Precocious puberty (links | edit)
- Delayed puberty (links | edit)
- Hypogonadism (links | edit)
- Hyperandrogenism (links | edit)
- Bicalutamide (links | edit)
- Xenoestrogen (links | edit)
- Hypoestrogenism (links | edit)
- Testotoxicosis (redirect page) (links | edit)
- Primary ovarian insufficiency (links | edit)
- Partial androgen insensitivity syndrome (links | edit)
- Estrogen insensitivity syndrome (links | edit)
- Endocrine disease (links | edit)
- 17β-Hydroxysteroid dehydrogenase III deficiency (links | edit)
- Sertoli cell-only syndrome (links | edit)
- Familial male precocious puberty (redirect page) (links | edit)
- Ovarian disease (links | edit)
- Androgen-dependent condition (links | edit)
- Aromatase deficiency (links | edit)
- Postorgasmic illness syndrome (links | edit)
- Hypergonadism (links | edit)
- Complete androgen insensitivity syndrome (links | edit)
- Hyperthecosis (links | edit)
- Intersex (links | edit)
- Mild androgen insensitivity syndrome (links | edit)
- Aromatase excess syndrome (links | edit)
- Hypergonadotropic hypogonadism (links | edit)
- Inborn errors of steroid metabolism (links | edit)
- Hyperestrogenism (links | edit)
- Leydig cell hypoplasia (links | edit)
- Male-limited precocious puberty (redirect page) (links | edit)
- Genetic disorder (links | edit)
- Achondroplasia (links | edit)
- Cenani–Lenz syndactylism (links | edit)
- Hirschsprung's disease (links | edit)
- Congenital hypothyroidism (links | edit)
- Osteopetrosis (links | edit)
- Gastrointestinal stromal tumor (links | edit)
- Waardenburg syndrome (links | edit)
- Hereditary hemorrhagic telangiectasia (links | edit)
- Ketoconazole (links | edit)
- Glanzmann's thrombasthenia (links | edit)
- Persistent Müllerian duct syndrome (links | edit)
- Kallmann syndrome (links | edit)
- Congenital insensitivity to pain with anhidrosis (links | edit)
- Crouzon syndrome (links | edit)
- Aspirin-exacerbated respiratory disease (links | edit)
- Apert syndrome (links | edit)
- Thanatophoric dysplasia (links | edit)
- Leber congenital amaurosis (links | edit)
- Hypogammaglobulinemia (links | edit)
- Hypochondroplasia (links | edit)
- Common variable immunodeficiency (links | edit)
- ABCD syndrome (links | edit)
- Jackson–Weiss syndrome (links | edit)
- Pfeiffer syndrome (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- Pseudohypoparathyroidism (links | edit)
- Familial male-limited precocious puberty (links | edit)
- X-linked severe combined immunodeficiency (links | edit)
- Selective immunoglobulin A deficiency (links | edit)
- Nevoid basal-cell carcinoma syndrome (links | edit)
- Piebaldism (links | edit)
- Robinow syndrome (links | edit)
- XX gonadal dysgenesis (links | edit)
- TNF receptor associated periodic syndrome (links | edit)
- Loeys–Dietz syndrome (links | edit)
- Hypohidrotic ectodermal dysplasia (links | edit)
- Familial hypercholesterolemia (links | edit)
- Jansen's metaphyseal chondrodysplasia (links | edit)
- Juvenile polyposis syndrome (links | edit)
- Laron syndrome (links | edit)
- Muenke syndrome (links | edit)
- Rabson–Mendenhall syndrome (links | edit)
- WHIM syndrome (links | edit)
- Antley–Bixler syndrome (links | edit)
- Congenital amegakaryocytic thrombocytopenia (links | edit)
- Worth syndrome (links | edit)
- Familial hypocalciuric hypercalcemia (links | edit)
- Leukocyte adhesion deficiency-1 (links | edit)
- Surfactant metabolism dysfunction (links | edit)
- Achondroplasia in children (links | edit)
- Donnai–Barrow syndrome (links | edit)
- Familial exudative vitreoretinopathy (links | edit)
- Donohue syndrome (links | edit)
- Leydig cell hypoplasia (links | edit)
- Gonadotropin-releasing hormone insensitivity (links | edit)
- Follicle-stimulating hormone insensitivity (links | edit)
- Gonadotropin insensitivity (links | edit)
- User:AleLopez14/sandbox (links | edit)
- User:Gibso.danny/sandbox (links | edit)
- User:Janeannyoung/sandbox (links | edit)
- User:Pdesai93/sandbox (links | edit)
- User:Egeorge01/sandbox (links | edit)
- User:Isaacadu1/sandbox (links | edit)
- User:Dmil3422/Laron Syndrome (links | edit)
- User talk:Pierlot (links | edit)
- Template:Cell surface receptor deficiencies (links | edit)
- Hypogonadotropic hypogonadism (links | edit)
- Androgen deficiency (links | edit)
- Fertile eunuch syndrome (links | edit)
- Estrogen-dependent condition (links | edit)
- Premature thelarche (links | edit)
- Gonadotropin-independent precocious puberty (redirect page) (links | edit)
- Gonadotropin insensitivity (links | edit)
- Medical uses of bicalutamide (links | edit)
- Hypergonadotropic hypergonadism (links | edit)
- Cytochrome b5 deficiency (links | edit)
- Cytochrome P450 oxidoreductase deficiency (links | edit)
- Precocious puberty, male limited (redirect page) (links | edit)
- Patrick Burleigh (links | edit)
- Talk:Familial male-limited precocious puberty (transclusion) (links | edit)