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question status | Tabled | ||||||||||
answering dept id | 17 | ||||||||||
answering dept short name | Health | ||||||||||
answering dept sort name | Health | ||||||||||
hansard heading | Hereditary Diseases | ||||||||||
house id | 2 | ||||||||||
identifier | HL5893 | ||||||||||
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parliament number | 55 | ||||||||||
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question text | To ask Her Majesty’s Government which government department or organisation or body in the National Health Service is currently responsible for setting or determining the national policy for carrier screening for (1) Tay Sachs disease, (2) Familial Dysautonomia and Canavan disease, and (3) other severe inherited genetic disorders, in at risk populations without an established family history. | ||||||||||
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session number | 4 | ||||||||||
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title | House of Lords Tabled Parliamentary Question 2014/15 HL5893 | ||||||||||
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uin | HL5893 | ||||||||||
version | 1 | ||||||||||
written parliamentary question type | Ordinary | ||||||||||
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question status | Tabled | ||||||||||
answering dept id | 17 | ||||||||||
answering dept short name | Health | ||||||||||
answering dept sort name | Health | ||||||||||
hansard heading | Hereditary Diseases | ||||||||||
house id | 2 | ||||||||||
identifier | HL5894 | ||||||||||
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parliament number | 55 | ||||||||||
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question text | To ask Her Majesty’s Government which government department, NHS organisation or body is currently responsible for commissioning carrier screening services for (1) Tay Sachs disease, (2) Familial Dysautonomia and Canavan disease, and (3) other severe inherited genetic disorders, in at risk populations without an established family history. | ||||||||||
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session number | 4 | ||||||||||
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title | House of Lords Tabled Parliamentary Question 2014/15 HL5894 | ||||||||||
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uin | HL5894 | ||||||||||
version | 1 | ||||||||||
written parliamentary question type | Ordinary | ||||||||||
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question status | Tabled | ||||||||||
answering dept id | 17 | ||||||||||
answering dept short name | Health | ||||||||||
answering dept sort name | Health | ||||||||||
hansard heading | Hereditary Diseases | ||||||||||
house id | 2 | ||||||||||
identifier | HL5891 | ||||||||||
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parliament number | 55 | ||||||||||
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question text | To ask Her Majesty’s Government which organisation or body is responsible for assessing the needs of the local population for carrier screening for genetic disorders in at risk populations without an established family history. | ||||||||||
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session number | 4 | ||||||||||
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title | House of Lords Tabled Parliamentary Question 2014/15 HL5891 | ||||||||||
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uin | HL5891 | ||||||||||
version | 1 | ||||||||||
written parliamentary question type | Ordinary | ||||||||||
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question status | Tabled | ||||||||||
answering dept id | 17 | ||||||||||
answering dept short name | Health | ||||||||||
answering dept sort name | Health | ||||||||||
hansard heading | Hereditary Diseases | ||||||||||
house id | 2 | ||||||||||
identifier | HL854 | ||||||||||
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parliament number | 55 | ||||||||||
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question text | To ask Her Majesty’s Government, further to the Written Answer by Earl Howe on 1 April (WA 178), whether they intend to issue a clarification of the differences between the figures for the number of babies born with mitochondrial disorders in their press releases on 28 June 2013 and 27 February 2014; whether the updated disease estimate for the United Kingdom based both on data from the 2011 census and observational epidemiological studies from the north-east of England is closer to their stated figure of one in 6,500 or one in 200; what was the corresponding frequency of children in either the north-east of England or the United Kingdom as a whole that were diagnosed with each of the mitochondrial diseases listed in Annex D of the consultation document entitled "Mitochondrial Donation" over the last ten years for which data are available; and how those figures compare to available data on population frequencies for mutations within the nuclear POLG1 and POLG2 genes. | ||||||||||
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session number | 4 | ||||||||||
tabling member printed |
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title | House of Lords Tabled Parliamentary Question 2014/15 HL854 | ||||||||||
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uin | HL854 | ||||||||||
version | 2 | ||||||||||
written parliamentary question type | Ordinary | ||||||||||
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question status | Tabled | ||||||||||
answering dept id | 17 | ||||||||||
answering dept short name | Health and Social Care | ||||||||||
answering dept sort name | Health and Social Care | ||||||||||
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hansard heading | Hereditary Diseases | ||||||||||
house id | 2 | ||||||||||
identifier | HL8241 | ||||||||||
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parliament number | 58 | ||||||||||
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question text | To ask His Majesty's Government, further to the Written Answer by Earl Howe on 15 July 2013 (HL1303), what progress the Human and Embryology Authority is able to report that may correspond to previous estimates that mitochondria replacement techniques could "save the lives of up to 10 babies who are born every year with a severe form of the disease, such as those with high levels of mutations". | ||||||||||
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session number | 3 | ||||||||||
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title | House of Lords Tabled Parliamentary Question 2022/23 HL8241 | ||||||||||
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uin | HL8241 | ||||||||||
version | 1 | ||||||||||
written parliamentary question type | Ordinary | ||||||||||
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question status | Tabled | ||||||||||
answering dept id | 53 | ||||||||||
answering dept short name | Cabinet Office | ||||||||||
answering dept sort name | Cabinet Office | ||||||||||
hansard heading | Hereditary Diseases | ||||||||||
house id | 1 | ||||||||||
identifier | 211015 | ||||||||||
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parliament number | 55 | ||||||||||
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question text | To ask the Minister for the Cabinet Office, how many infant deaths were caused by MCAD deficiency in (a) East Lancashire, (b) the North West and (c) England in each of the last three years. | ||||||||||
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session number | 4 | ||||||||||
tabling member constituency | Pendle | ||||||||||
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title | House of Commons Tabled Parliamentary Question 2014/15 211015 | ||||||||||
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uin | 211015 | ||||||||||
version | 2 | ||||||||||
written parliamentary question type | Ordinary | ||||||||||
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question status | Tabled | ||||||||||
answering dept id | 17 | ||||||||||
answering dept short name | Health and Social Care | ||||||||||
answering dept sort name | Health and Social Care | ||||||||||
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hansard heading | Hereditary Diseases | ||||||||||
house id | 1 | ||||||||||
identifier | 40538 | ||||||||||
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parliament number | 58 | ||||||||||
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question text | To ask the Secretary of State for Health and Social Care, what recent progress his Department has made on research into the treatment of mitochondrial disease. | ||||||||||
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session number | 1 | ||||||||||
tabling member constituency | The Wrekin | ||||||||||
tabling member printed |
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title | House of Commons Tabled Parliamentary Question 2019/21 40538 | ||||||||||
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uin | 40538 | ||||||||||
version | 1 | ||||||||||
written parliamentary question type | Ordinary | ||||||||||
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answering body |
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question status | Tabled | ||||||||||
answering dept id | 17 | ||||||||||
answering dept short name | Health and Social Care | ||||||||||
answering dept sort name | Health and Social Care | ||||||||||
ddp modified |
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hansard heading | Hereditary Diseases | ||||||||||
house id | 1 | ||||||||||
identifier | 183532 | ||||||||||
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parliament number | 58 | ||||||||||
question first answered |
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question text | To ask the Secretary of State for Health and Social Care, what steps his Department is taking to support people with undiagnosed genetic conditions. | ||||||||||
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session number | 3 | ||||||||||
tabling member constituency | Blaydon | ||||||||||
tabling member printed |
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title | House of Commons Tabled Parliamentary Question 2022/23 183532 | ||||||||||
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uin | 183532 | ||||||||||
version | 1 | ||||||||||
written parliamentary question type | NamedDay | ||||||||||
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answering body |
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question status | Tabled | ||||||||||
answering dept id | 17 | ||||||||||
answering dept short name | Health | ||||||||||
answering dept sort name | Health | ||||||||||
hansard heading | Hereditary Diseases | ||||||||||
house id | 1 | ||||||||||
identifier | 226013 | ||||||||||
legislature |
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parliament number | 55 | ||||||||||
question first answered |
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question text | To ask the Secretary of State for Health, pursuant to the Answer of 3 March 2015 to Question 225464, if he will estimate the annual cost to the NHS of the implications of genetic inheritance birth defects. | ||||||||||
session |
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session number | 4 | ||||||||||
tabling member constituency | Shipley | ||||||||||
tabling member printed |
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title | House of Commons Tabled Parliamentary Question 2014/15 226013 | ||||||||||
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uin | 226013 | ||||||||||
version | 1 | ||||||||||
written parliamentary question type | Ordinary | ||||||||||
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answering body |
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question status | Tabled | ||||||||||
answering dept id | 17 | ||||||||||
answering dept short name | Health | ||||||||||
answering dept sort name | Health | ||||||||||
hansard heading | Hereditary Diseases | ||||||||||
house id | 1 | ||||||||||
identifier | 225464 | ||||||||||
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parliament number | 55 | ||||||||||
question first answered |
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question text | To ask the Secretary of State for Health, what assessment his Department has made of the health effects of consanguineous marriages; and what steps he is taking to reduce them. | ||||||||||
session |
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session number | 4 | ||||||||||
tabling member constituency | Shipley | ||||||||||
tabling member printed |
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title | House of Commons Tabled Parliamentary Question 2014/15 225464 | ||||||||||
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uin | 225464 | ||||||||||
version | 2 | ||||||||||
written parliamentary question type | Ordinary | ||||||||||
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