New Cosponsor — Sep 10, 2012
New Cosponsor: Rep. Christopher “Chris” Smith [R-NJ4]
The bill now has 34 cosponsors (26 Democrats, 8 Republicans).
Jun 3, 2011
112th Congress, 2011–2013
This bill was introduced on June 3, 2011, in a previous session of Congress, but was not enacted.
Representative for California's 24th congressional district
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Last Updated: Jun 3, 2011
Length: 16 pages
To amend the Public Health Service Act to improve the diagnosis and treatment of hereditary hemorrhagic telangiectasia, and for other purposes.
6/3/2011--Introduced.Hereditary Hemorrhagic Telangiectasia Diagnosis and Treatment Act of 2011 - Amends the Public Health Service Act to require the Secretary of Health and Human Services (HHS) to establish and implement ... Read more >
The bill’s title was written by its sponsor.
This is the first step in the legislative process.
This is a House of Representatives bill in the United States Congress (indicated by the “H.R.” in “H.R. 2123”). A bill must be passed by both the House and Senate in identical form and then be signed by the President to become law.
There have been no roll call votes related to this bill.
Click a format for a citation suggestion:
Civic Impulse. (2015). H.R. 2123 — 112th Congress: Hereditary Hemorrhagic Telangiectasia Diagnosis and Treatment Act of 2011. Retrieved from https://www.govtrack.us/congress/bills/112/hr2123
“H.R. 2123 — 112th Congress: Hereditary Hemorrhagic Telangiectasia Diagnosis and Treatment Act of 2011.” www.GovTrack.us. 2011. November 29, 2015 <https://www.govtrack.us/congress/bills/112/hr2123>
|title=H.R. 2123 (112th)
|accessdate=November 29, 2015
|author=112th Congress (2011)
|date=June 3, 2011
|quote=Hereditary Hemorrhagic Telangiectasia Diagnosis and Treatment Act of 2011