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2,925 Possible Causes for Chronic Fatigue Syndrome, Kallmann Syndrome, Mutation in the KISS1 Receptor Gene

  • Primary Male Hypogonadism

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

  • 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]

  • Anterior Pituitary Hypofunction

    syndrome (hypogonadotropic hypogonadism with anosmia) 253.4 Syndrome - see also Disease Kallmann's (hypogonadotropic hypogonadism with anosmia) 253.4 Crosswalk Information[healthprovidersdata.com] […] hormone Isolated deficiency of pituitary hormone Kallmann's syndrome Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary cachexia[icd10data.com] syndrome Lymphocytic hypophysitis Transsphenoidal adenomectomy Congenital - Usually presents in childhood, but can present later with features such as delayed puberty; heritable[emedicine.medscape.com]

    Missing: Mutation in the KISS1 Receptor Gene
  • 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: Chronic Fatigue Syndrome
  • 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: Chronic Fatigue Syndrome
  • Panhypopituitarism

    Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of gonadotropin Isolated deficiency of growth hormone Isolated deficiency of pituitary hormone Kallmann's[icd10data.com] syndrome Lymphocytic hypophysitis Transsphenoidal adenomectomy Congenital - Usually presents in childhood, but can present later with features such as delayed puberty; heritable[emedicine.medscape.com] A genetic syndrome that is associated with panhypopituitarism is the Kallmann's syndrome.[lifepersona.com]

    Missing: Mutation in the KISS1 Receptor Gene
  • Ayerza Syndrome

    , see ophthalmo-acromelic syndrome anosmic hypogonadism, see Kallmann syndrome anosmic idiopathic hypogonadotropic hypogonadism, see Kallmann syndrome ANS, see ataxia neuropathy[mygenomics.com] Blizzard K Kahler's disease – Otto Kahler Kallmann syndrome – Franz Josef Kallmann Kanner syndrome – Leo Kanner Kaposi sarcoma – Moritz Kaposi Kartagener syndrome – Manes[ipfs.io] Blizzard Julian syndrome - Frankie Julian, Ron Kendall, Abe Charara K Kahler's disease - Otto Kahler Kallmann syndrome - Franz Josef Kallmann Kanner syndrome - Leo Kanner[like2do.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] Xq28 Duplication Syndrome chronic atrial and intestinal dysrhythmia chronic fatigue syndrome Chudley-Mccullough syndrome Chudley-Rozdilsky Syndrome Churg-Strauss syndrome[rgd.mcw.edu] 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]

  • Kallmann Syndrome Type 3

    gene (KISS1 receptor product)?[quizlet.com] […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] Kallmann syndrome.[misc.medscape.com]

    Missing: Chronic Fatigue Syndrome
  • Spastic Paraparesis-Deafness Syndrome

    These include criteria for the diagnosis of multiple sclerosis, dementia of Lewy-body type, frontal lobe dementias, chronic fatigue syndrome, and inflammatory neuropathies[books.google.com] Back to: « Kallmann syndrome Symptoms of Kallmann syndrome with spastic paraplegia Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of head or[familydiagnosis.com] […] cyst Autosomal dominant intermediate Charcot-Marie-Tooth Curry Jones syndrome Kallmann syndrome 1 Upington disease X-linked adrenal hypoplasia congenita Ichthyosis lamellar[checkrare.com]

    Missing: Mutation in the KISS1 Receptor Gene