Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 15 for Autosomal dominant osteoporosis 2
  1. Dyskeratosis congenita 
    ... DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 3; DKCB3 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3 DYSKERATOSIS ...
    https://medlineplus.gov/genetics/condition/dyskeratosis-congenita - Genetics
  2. Severe congenital neutropenia 
    ... CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5 NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT; SCN2 NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE; SCN7 ...
    https://medlineplus.gov/.../condition/severe-congenital-neutropenia - Genetics
  3. CASR gene 
    ... sensing receptors determine clinical presentations in patients with autosomal dominant hypocalcemia. J Clin Endocrinol Metab. 2014 Feb;99(2):E363-8. doi: 10.1210/jc.2013-3430. ...
    https://medlineplus.gov/genetics/gene/casr - Genetics
  4. LRP5 gene 
    ... LRP5 gene may influence the risk of developing osteoporosis in adulthood. ... dominant osteopetrosis type 1 and autosomal dominant osteosclerosis. In ...
    https://medlineplus.gov/genetics/gene/lrp5 - Genetics
  5. Hajdu-Cheney syndrome 
    ... condition. NOTCH2 ... Acroosteolysis dominant type Acroosteolysis with osteoporosis and changes in skull and mandible Arthro-dento- ...
    https://medlineplus.gov/genetics/condition/hajdu-cheney-syndrome - Genetics
  6. Hyperparathyroidism-jaw tumor syndrome 
    ... unknown. CDC73 ... Genetic Testing Registry: Hyperparathyroidism 2 with jaw tumors ...
    https://medlineplus.gov/.../hyperparathyroidism-jaw-tumor-syndrome - Genetics
  7. FLNB gene 
    ... Robertson SP, Cohn DH, Krakow D. Mutations in two regions of FLNB result in ... synostosis syndrome: phenotypic homogeneity and genetic heterogeneity. ...
    https://medlineplus.gov/genetics/gene/flnb - Genetics
  8. Williams Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    National Institute of Neurological Disorders and Stroke ... Genetic Disorders/Specifics ... Genetic Disorders ... Developmental Disabilities/Specifics ... Developmental Disabilities
    https://www.ninds.nih.gov/.../disorders/williams-syndrome - External Health Links
  9. Familial exudative vitreoretinopathy 
    ... the FZD4 or LRP5 gene and has an autosomal dominant pattern of inheritance. Autosomal dominant inheritance means one copy of the altered gene ... sufficient to cause the disorder. Most people with autosomal dominant familial exudative vitreoretinopathy inherit the altered gene from ...
    https://medlineplus.gov/.../familial-exudative-vitreoretinopathy - Genetics
  10. Mineral and Bone Disorder in Chronic Kidney Disease From the National Institutes of Health (National Institute of Diabetes and Digestive and Kidney Diseases)  
    National Institute of Diabetes and Digestive and Kidney Diseases ... Dialysis/Related Issues ... Dialysis ... Kidney Failure/Related Issues ... Kidney Failure ... Parathyroid ...
    https://www.niddk.nih.gov/.../kidney-disease/mineral-bone-disorder - External Health Links
previous · 1 · 2 · next