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177 Possible Causes for Hypertrichosis of Upper Back, Hypoplastic Testicle, Prominent High Nasal Root

  • Warburg Micro Syndrome 3

    Finding useful health information on the Internet can be difficult, but we’re here to help. This page gathers quality information from trusted sources. You can learn more about the disease, visit handpicked websites, and find resources to help you in your daily life. Need more information? Click the menu on the left[…][resourcerepository.org]

    Missing: Prominent High Nasal Root
  • Woodhouse Sakati Syndrome

    nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Prominent[rarediseases.info.nih.gov] […] forehead, flattened occiput, triangular face, prominent nasal root, hypertelorism, downward slanting palpebral fissures), scoliosis, hyperreflexia and camptodactyly.[sites.uclouvain.be] […] forehead, flat occiput, triangular face, prominent nasal root, hypertelorism, and down-slanting palpebral fissures), scoliosis, hyperreflexia, and camptodactyly.[rarediseases.info.nih.gov]

    Missing: Hypertrichosis of Upper Back
  • Schwartz-Jampel Syndrome

    nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Ptosis[rarediseases.info.nih.gov] Nearsightedness [ more ] 0000545 Osteoporosis 0000939 Overfolded helix Overfolded ears 0000396 Pectus carinatum Pigeon chest 0000768 Platyspondyly Flattened vertebrae 0000926 Prominent[rarediseases.info.nih.gov]

    Missing: Hypertrichosis of Upper Back
  • Renpenning Syndrome

    He shows large, low-set ears, high nasal root, micrognathia, long philtrum, and prominent metopic suture.[doi.org]

    Missing: Hypertrichosis of Upper Back
  • Hypogonadotropic Hypogonadism Type 22

    Mikelsaar, Ruth, Lissitsina, Jelena, Bartsch, Oliver Source: Journal of applied genetics 2011 v.52 no.3 pp. 331-334 ISSN: 1234-1983 Subject: chromosomes, humans, spermatogenesis Abstract: We describe the first case of a supernumerary inv dup(22)(q11.1) in an infertile male with hypogonadotropic hypogonadism. This case[…][pubag.nal.usda.gov]

    Missing: Hypertrichosis of Upper Back Prominent High Nasal Root
  • Kallmann Syndrome Type 4

    […] doi: 10.1097/01.XHA.0000479441.49042.58 Review articles Abstract Author Information Authors Article Metrics Metrics Delayed, failed, or arrested puberty is the consequence of hypogonadism among adolescent boys. A variety of congenital and acquired conditions that affect the hypothalamus and/or the pituitary gland[…][journals.lww.com]

    Missing: Hypertrichosis of Upper Back Prominent High Nasal Root
  • Hypogonadotropic Hypogonadism Type 8

    OMIM : 57 Congenital idiopathic hypogonadotropic hypogonadism (IHH) is a disorder characterized by absent or incomplete sexual maturation by the age of 18 years, in conjunction with low levels of circulating gonadotropins and testosterone and no other abnormalities of the hypothalamic-pituitary axis. Idiopathic[…][malacards.org]

    Missing: Hypertrichosis of Upper Back Prominent High Nasal Root
  • Brandt Syndrome

    From Wikidata Jump to navigation Jump to search Human disease Acrodermatitis enteropathica, zinc deficiency type Acrodermatitis enteropathica zinc deficiency type Inherited zinc deficiency Danbolt-Cross syndrome ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE; AEZ Brandt syndrome AE ACRODERMATITIS[…][wikidata.org]

    Missing: Hypertrichosis of Upper Back Prominent High Nasal Root
  • Moebius Syndrome

    The clinicopathological findings on a 17-year-old female with the Möbius/Moebius syndrome are reported. The signs and symptoms of this neuromuscular condition include congenital bilateral or unilateral palsies of the facial and abducens cranial nerves and a broad scope of multisystem abnormalities. A case of unilateral[…][ncbi.nlm.nih.gov]

    Missing: Hypertrichosis of Upper Back Prominent High Nasal Root
  • Factor XIII Deficiency

    From Wikidata Jump to navigation Jump to search Human disease factor XIII deficiency deficiency, Laki-Lorand factor factor XIII deficiency disease (disorder) hereditary factor XIII deficiency disease (disorder) Hereditary factor XIII deficiency disease Factor XIII deficiency disease Fibrin-stabilizing factor deficiency[…][wikidata.org]

    Missing: Hypertrichosis of Upper Back Prominent High Nasal Root