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2,459 Possible Causes for Dysautonomia, Kallmann Syndrome, Mutation in the KISS1 Receptor Gene

  • Primary Male Hypogonadism

    gene (KISS1 receptor product)?[quizlet.com] Secondary hypogonadism can be caused by Kallmann syndrome, pituitary or hypothalamic tumors or disorders, obesity, diabetes and Prader-Willi syndrome.[froedtert.com] A number of conditions can cause secondary hypogonadism, including: Kallmann syndrome.[mayoclinic.org]

  • Male Hypogonadism

    gene (KISS1 receptor product)?[quizlet.com] Disorders Causing Pituitary Hypogonadism Brain and pituitary tumors Hemochromatosis Kallmann syndrome Weight loss Obesity Diabetes Testicular Disorders Causing Hypogonadism[louisville.edu] Certain conditions such as Kallmann syndrome (abnormal development of the hypothalamus), pituitary disorders, inflammatory diseases, HIV, certain medications, obesity and[uhs.ae]

  • Leydig Cell Hypoplasia due to LHB Deficiency

    Mutations of the GnRH1 gene have also been reported in patients with hypogonadotropic hypogonadism, although they are rare.[clinicalgate.com] syndrome and GnRH insensitivity[en.wikipedia.org] […] with resp. distress 1 IGHMBP2 Immunoglobulin K deficiency IGKV@ Agammaglobulinaemia, autosomal recessive IGLL1 Brachydactyly type A1 IHH Acrocapitofemoral dysplasia IHH Dysautonomia[springer.com]

  • Hypogonadotropic Hypogonadism Type 8

    Mutations involving the genes GnRH1 and KISS1, are a very rare cause of HH [41], [42].[journals.plos.org] Kallmann syndrome - absent puberty with no sense of smell. Me at 18 years old in my final year at school. I had not started puberty yet.[imgur.com] Anosmia is a distinguishing characteristic of Kallmann syndrome from other subtypes of IHH.[omicsonline.org]

    Missing: Dysautonomia
  • Hypogonadism

    […] in the genes encoding GNRH1 or its receptor will result in the failure of the HPG axis and give rise to normosmic CHH. [2] Inactivating mutations of KISS1 or KISS1R causes[en.wikipedia.org] BACKGROUND: Congenital hypogonadotrophic hypogonadism (CHH) and Kallmann syndrome (KS) are caused by disruption to the hypothalamic-pituitary-gonadal (H-P-G) axis.[ncbi.nlm.nih.gov] Kallmann syndrome) as well as normal puberty that is accompanied by an altered reproductive system later in life (i.e. ...[centerwatch.com]

    Missing: Dysautonomia
  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    Mutations involving the genes GnRH1 and KISS1, are a very rare cause of HH [41], [42].[journals.plos.org] Anosmia is a distinguishing characteristic of Kallmann syndrome from other subtypes of IHH.[omicsonline.org] […] resistance to) IGHM (Agammaglobulinemia 1) IGHMBP2 (Neuronopathy, distal hereditary motor, type VI) IGLL1 (Agammaglobulinemia 2) IHH (Acrocapitofemoral dysplasia) IKBKAP (Dysautonomia[en.praenatal-medizin.de]

  • Melhem-Fahl Syndrome

    syndrome Kaler Garrity Stern Syndrome Kallmann syndrome Kantaputra Gorlin Syndrome Kaplan Plauchu Fitch Syndrome Kaplowitz Bodurtha syndrome Kapur Toriello Syndrome Karak[rgd.mcw.edu] Association Pilotto Syndrome Piussan Lenaerts Mathieu Syndrome Podder-Tolmie Syndrome Polydactyly Polyhydramnios Postthrombotic Syndrome Preeyasombat Varavithya Syndrome Primary Dysautonomias[empiregenomics.com] Rizzo Syndrome PHACE Association Pilotto Syndrome Piussan Lenaerts Mathieu Syndrome Podder-Tolmie Syndrome Postthrombotic Syndrome Preeyasombat Varavithya Syndrome Primary Dysautonomias[empiregenomics.com]

    Missing: Mutation in the KISS1 Receptor Gene
  • Isolated Follicle Stimulating Hormone Deficiency

    Their endogenous gonadotropin secretion was compared with that of two other infertile men with hypothalamic disease (Kallmann's syndrome) and pituitary tumor with hyperprolactinemia[ncbi.nlm.nih.gov] Funding and Disclosures Supported in part by grants from the Israel Cancer Society, the Dysautonomia Society and the Joint Fund Hadassah–Hebrew University.[nejm.org] This disorder featuring lack of sense of smell is called anosmia or Kallmann syndrome.[healthhype.com]

    Missing: Mutation in the KISS1 Receptor Gene
  • Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome

    […] in the genes encoding GNRH1 or its receptor will result in the failure of the HPG axis and give rise to normosmic CHH. [2] Inactivating mutations of KISS1 or KISS1R causes[en.wikipedia.org] […] with or without polydactyly 611263 IGHMBP2 11q13.3 Charcot-Marie-Tooth disease, axonal, type 2S 616155 Neuronopathy, distal hereditary motor, type VI 604320 IKBKAP 9q31.3 Dysautonomia[institutobernabeu.com] Polycystic ovary syndrome, and Kallmann syndrome, also called hypogonadotropic hypogonadism. [1] Hemochromatosis and diabetes mellitus can be causes of this as well.[en.wikipedia.org]

  • Congenital Absence of the Penis

    Mutations involving the genes GnRH1 and KISS1, are a very rare cause of HH [41], [42].[journals.plos.org] As with a lot (but not all) men with Kallmann syndrome I have underdeveloped genitals.[kallmannsyndrome.wordpress.com] .: familial dysautonomia (K07.-) malformation syndromes affecting facial appearance (Q87.0) persistent thyroglossal duct (Q89.2) Q18.0 Sinus, fistula and cyst of branchial[embryology.med.unsw.edu.au]

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