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 163 for cd
  1. AQP2 gene 
    ... Health Condition ADH water channel AQP-2 AQP-CD AQP2_HUMAN aquaporin 2 (collecting duct) aquaporin-2 aquaporin-CD collecting duct water channel protein MGC34501 water channel ...
    https://medlineplus.gov/genetics/gene/aqp2 - Genetics
  2. Chanarin-Dorfman syndrome 
    ... not show signs and symptoms of the condition. CDS Chanarin-Dorfman disease DCS Dorfman-Chanarin disease Dorfman- ... Rare Disorders (NORD) ClinicalTrials.gov CHANARIN-DORFMAN SYNDROME; CDS PubMed Bruno C, Bertini E, Di Rocco M, ...
    https://medlineplus.gov/genetics/condition/chanarin-dorfman-syndrome - Genetics
  3. Cowden syndrome 
    ... no history of the disorder in their family. CD Cowden disease Cowden's disease Cowden's syndrome ...
    https://medlineplus.gov/genetics/condition/cowden-syndrome - Genetics
  4. SLC5A1 gene 
    ... D22S675 Human Na+/glucose cotransporter 1 mRNA, complete cds NAGT SC5A1_HUMAN SGLT1 solute carrier family 5 ( ...
    https://medlineplus.gov/genetics/gene/slc5a1 - Genetics
  5. Blau syndrome 
    ... berh.2011.10.017. Citation on PubMed Rose CD, Arostegui JI, Martin TM, Espada G, Scalzi L, ... PubMed or Free article on PubMed Central Rose CD, Doyle TM, McIlvain-Simpson G, Coffman JE, Rosenbaum ...
    https://medlineplus.gov/genetics/condition/blau-syndrome - Genetics
  6. Pachyonychia congenita 
    ... MJ, Leachman SA, Feng BJ, Schwartz ME, Hansen CD. A review of the clinical phenotype of 254 ... Jan 20. Citation on PubMed McLean WH, Hansen CD, Eliason MJ, Smith FJ. The phenotypic and molecular ...
    https://medlineplus.gov/genetics/condition/pachyonychia-congenita - Genetics
  7. Inherited thyroxine-binding globulin deficiency 
    ... thyroxine-binding globulin deficiency: the complete form (TBG-CD), which results in a total loss of thyroxine- ... form of inherited thyroxine-binding globulin deficiency, TBG-CD, affects about 1 in 15,000 newborns worldwide. ...
    https://medlineplus.gov/...ted-thyroxine-binding-globulin-deficiency - Genetics
  8. X-linked creatine deficiency 
    ... S, Sargent M, Stockler-Ipsiroglu S, van Karnebeek CD. Treatment of X-linked creatine transporter (SLC6A8) deficiency: ... Citation on PubMed Stockler-Ipsiroglu S, van Karnebeek CD. Cerebral creatine deficiencies: a group of treatable intellectual ...
    https://medlineplus.gov/.../condition/x-linked-creatine-deficiency - Genetics
  9. Hand-foot-genital syndrome 
    ... Z, Ludwig M, Williams ME, Williams TM, Doyle CD, Shao Z, Glynn M, Mikulic D, Lehmann K, ... Oct 29. Citation on PubMed Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dotsch J, ...
    https://medlineplus.gov/.../condition/hand-foot-genital-syndrome - Genetics
  10. Miller syndrome 
    ... C, Bigham AW, Tabor HK, Dent KM, Huff CD, Shannon PT, Jabs EW, Nickerson DA, Shendure J, ... Central Roach JC, Glusman G, Smit AF, Huff CD, Hubley R, Shannon PT, Rowen L, Pant KP, ...
    https://medlineplus.gov/genetics/condition/miller-syndrome - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next