All individuals with variants in gene PITPNM3

Legend

Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

ID_report: ID of the individual that can be publically shared, e.g. as listed in a publication

Reference: reference to publication describing the individual/family, possibly giving more phenotypic details than listed in this database entry, incl. link to PubMed or other source, e.g. "den Dunnen ASHG2003 P2346"

Remarks: remarks about the individual

Gender: gender individual
All options:

? = unknown
- = not applicable
F = female
M = male
rF = raised as female
rM = raised as male

Consanguinity: indicates whether the parents are related (consanguineous), not related (non-consanguineous) or whether consanguinity is not known (unknown)
All options:

no = non-consanguineous parents
yes = consanguineous parents
likely = consanguinity likely
? = unknown
- = not applicable

Country: where (country) does the individual live/recently came from. Give additional details (population, specific sub-group) and when parents come from different countries in "Population". Belgium = individual lives in/recently came from Belgium, (France) = reported by laboratory in France, individual's country of origin not sure
All options:

? (unknown)
- (not applicable)
Afghanistan
(Afghanistan)
Albania
(Albania)
Algeria
(Algeria)
American Samoa
(American Samoa)
Andorra
(Andorra)
Angola
(Angola)
Anguilla
(Anguilla)
Antarctica
(Antarctica)
Antigua and Barbuda
(Antigua and Barbuda)
Argentina
(Argentina)
Armenia
(Armenia)
Aruba
(Aruba)
Australia
(Australia)
Austria
(Austria)
Azerbaijan
(Azerbaijan)
Bahamas
(Bahamas)
Bahrain
(Bahrain)
Bangladesh
(Bangladesh)
Barbados
(Barbados)
Belarus
(Belarus)
Belgium
(Belgium)
Belize
(Belize)
Benin
(Benin)
Bermuda
(Bermuda)
Bhutan
(Bhutan)
Bolivia
(Bolivia)
Bosnia and Herzegovina
(Bosnia and Herzegovina)
Botswana
(Botswana)
Bouvet Island
(Bouvet Island)
Brazil
(Brazil)
British Indian Ocean Territory
(British Indian Ocean Territory)
Brunei Darussalam
(Brunei Darussalam)
Bulgaria
(Bulgaria)
Burkina Faso
(Burkina Faso)
Burundi
(Burundi)
Cambodia
(Cambodia)
Cameroon
(Cameroon)
Canada
(Canada)
Cape Verde
(Cape Verde)
Cayman Islands
(Cayman Islands)
Central African Republic
(Central African Republic)
Central Europe
Chad
(Chad)
Chile
(Chile)
China
(China)
Christmas Island
(Christmas Island)
Cocos (Keeling Islands)
(Cocos (Keeling Islands))
Colombia
(Colombia)
Comoros
(Comoros)
Congo
(Congo)
Cook Islands
(Cook Islands)
Costa Rica
(Costa Rica)
Cote D'Ivoire (Ivory Coast)
(Cote D'Ivoire (Ivory Coast))
Croatia (Hrvatska)
(Croatia (Hrvatska))
Cuba
(Cuba)
Cyprus
(Cyprus)
Czech Republic
(Czech Republic)
Denmark
(Denmark)
Djibouti
(Djibouti)
Dominica
(Dominica)
Dominican Republic
(Dominican Republic)
East Timor
(East Timor)
Ecuador
(Ecuador)
Egypt
(Egypt)
El Salvador
(El Salvador)
England
(England)
Equatorial Guinea
(Equatorial Guinea)
Eritrea
(Eritrea)
Estonia
(Estonia)
Ethiopia
(Ethiopia)
Falkland Islands (Malvinas)
(Falkland Islands (Malvinas))
Faroe Islands
(Faroe Islands)
Fiji
(Fiji)
Finland
(Finland)
France
(France)
Gabon
(Gabon)
Gambia
(Gambia)
Georgia
(Georgia)
Germany
(Germany)
Ghana
(Ghana)
Gibraltar
(Gibraltar)
Greece
(Greece)
Greenland
(Greenland)
Grenada
(Grenada)
Guadeloupe
(Guadeloupe)
Guam
(Guam)
Guatemala
(Guatemala)
Guiana, French
(Guiana, French)
Guinea
(Guinea)
Guinea-Bissau
(Guinea-Bissau)
Guyana
(Guyana)
Haiti
(Haiti)
Heard and McDonald Islands
(Heard and McDonald Islands)
Honduras
(Honduras)
Hong Kong
(Hong Kong)
Hungary
(Hungary)
Iceland
(Iceland)
India
(India)
Indonesia
(Indonesia)
Iran
(Iran)
Iraq
(Iraq)
Ireland
(Ireland)
Israel
(Israel)
Italy
(Italy)
Jamaica
(Jamaica)
Japan
(Japan)
Jordan
(Jordan)
Kazakhstan
(Kazakhstan)
Kenya
(Kenya)
Kiribati
(Kiribati)
Korea
(Korea)
Korea, North (People's Republic)
(Korea, North (People's Republic))
Korea, South (Republic)
(Korea, South (Republic))
Kosovo
(Kosovo)
Kuwait
(Kuwait)
Kyrgyzstan (Kyrgyz Republic)
(Kyrgyzstan (Kyrgyz Republic))
Laos
(Laos)
Latvia
(Latvia)
Lebanon
(Lebanon)
Lesotho
(Lesotho)
Liberia
(Liberia)
Libya
(Libya)
Liechtenstein
(Liechtenstein)
Lithuania
(Lithuania)
Luxembourg
(Luxembourg)
Macau
(Macau)
Macedonia
(Macedonia)
Madagascar
(Madagascar)
Malawi
(Malawi)
Malaysia
(Malaysia)
Maldives
(Maldives)
Mali
(Mali)
Mallorca
(Mallorca)
Malta
(Malta)
Marshall Islands
(Marshall Islands)
Martinique
(Martinique)
Mauritania
(Mauritania)
Mauritius
(Mauritius)
Mayotte
(Mayotte)
Mexico
(Mexico)
Micronesia
(Micronesia)
Moldova
(Moldova)
Monaco
(Monaco)
Mongolia
(Mongolia)
Montserrat
(Montserrat)
Morocco
(Morocco)
Mozambique
(Mozambique)
Myanmar
(Myanmar)
Namibia
(Namibia)
Nauru
(Nauru)
Nepal
(Nepal)
Netherlands
(Netherlands)
Netherlands Antilles
(Netherlands Antilles)
Neutral Zone (Saudia Arabia/Iraq)
(Neutral Zone (Saudia Arabia/Iraq))
New Caledonia
(New Caledonia)
New Zealand
(New Zealand)
Nicaragua
(Nicaragua)
Niger
(Niger)
Nigeria
(Nigeria)
Niue
(Niue)
Norfolk Island
(Norfolk Island)
Northern Ireland
(Northern Ireland)
Northern Mariana Islands
(Northern Mariana Islands)
Norway
(Norway)
Oman
(Oman)
Pakistan
(Pakistan)
Palau
(Palau)
Palestine
(Palestine)
Panama
(Panama)
Papua New Guinea
(Papua New Guinea)
Paraguay
(Paraguay)
Peru
(Peru)
Philippines
(Philippines)
Pitcairn
(Pitcairn)
Poland
(Poland)
Polynesia, French
(Polynesia, French)
Portugal
(Portugal)
Puerto Rico
(Puerto Rico)
Qatar
(Qatar)
Reunion
(Reunion)
Romania
(Romania)
Russia
(Russia)
Russian Federation
(Russian Federation)
Rwanda
(Rwanda)
S. Georgia and S. Sandwich Isls.
(S. Georgia and S. Sandwich Isls.)
Saint Kitts and Nevis
(Saint Kitts and Nevis)
Saint Lucia
(Saint Lucia)
Saint Vincent and The Grenadines
(Saint Vincent and The Grenadines)
Samoa
(Samoa)
San Marino
(San Marino)
Sao Tome and Principe
(Sao Tome and Principe)
Saudi Arabia
(Saudi Arabia)
Scotland
(Scotland)
Senegal
(Senegal)
Serbia
(Serbia)
Seychelles
(Seychelles)
Sierra Leone
(Sierra Leone)
Singapore
(Singapore)
Slovakia (Slovak Republic)
(Slovakia (Slovak Republic))
Slovenia
(Slovenia)
Solomon Islands
(Solomon Islands)
Somalia
(Somalia)
South Africa
(South Africa)
Southern Territories, French
(Southern Territories, French)
Soviet Union (former)
(Soviet Union (former))
Spain
(Spain)
Sri Lanka
(Sri Lanka)
St. Helena, Ascension and Tristan da
Cunha
(St. Helena, Ascension and Tristan da
Cunha)
St. Pierre and Miquelon
(St. Pierre and Miquelon)
Sudan
(Sudan)
Sudan, South
(Sudan, South)
Suriname
(Suriname)
Svalbard and Jan Mayen Islands
(Svalbard and Jan Mayen Islands)
Swaziland
(Swaziland)
Sweden
(Sweden)
Switzerland
(Switzerland)
Syria
(Syria)
Taiwan
(Taiwan)
Tajikistan
(Tajikistan)
Tanzania
(Tanzania)
Thailand
(Thailand)
Togo
(Togo)
Tokelau
(Tokelau)
Tonga
(Tonga)
Trinidad and Tobago
(Trinidad and Tobago)
Tunisia
(Tunisia)
Turkey
(Turkey)
Turkmenistan
(Turkmenistan)
Turks and Caicos Islands
(Turks and Caicos Islands)
Tuvalu
(Tuvalu)
Uganda
(Uganda)
Ukraine
(Ukraine)
United Arab Emirates
(United Arab Emirates)
United Kingdom (Great Britain)
(United Kingdom (Great Britain))
United States
(United States)
Uruguay
(Uruguay)
US Minor Outlying Islands
(US Minor Outlying Islands)
Uzbekistan
(Uzbekistan)
Vanuatu
(Vanuatu)
Vatican City State (Holy See)
(Vatican City State (Holy See))
Venezuela
(Venezuela)
Viet Nam
(Viet Nam)
Virgin Islands (British)
(Virgin Islands (British))
Virgin Islands (US)
(Virgin Islands (US))
Wales
(Wales)
Wallis and Futuna Islands
(Wallis and Futuna Islands)
Western Sahara
(Western Sahara)
Yemen
(Yemen)
Yugoslavia
(Yugoslavia)
Zaire
(Zaire)
Zambia
(Zambia)
Zimbabwe
(Zimbabwe)

Population: population the individual (or ancestors) belongs to; e.g. white, gypsy, Jewish-Ashkenazi, Africa-N, Sardinia, etc.

Age at death: age at which the individual deceased (when applicable):

35y = 35 years
>43y = still alive at 43y
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown

VIP: individual/phenotype VIP-status was requested for matchmaking - need collaboration(s) to crack the case - please contact the submitter/curator. NOTE: to get VIP status ask the curator.

Data_av: are additional data available upon request: e.g. pedigree (yes/no/?)

Treatment: treatment of patient

Variants in genes: The individual has variants for this gene.

Panel size: Number of individuals this entry represents; e.g. 1 for an individual, 5 for a family with 5 affected members.

How to query this table

All list views have search fields which can be used to search data. You can search for a complete word or you can search for a part of a search term. If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify. Note that search terms are case-insensitive and that wildcards such as * are treated as normal text! For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.

Operator	Column type	Example	Matches
	Text	Arg	all entries containing 'Arg'
space	Text	Arg Ser	all entries containing 'Arg' and 'Ser'
\|	Text	Arg\|Ser	all entries containing 'Arg' or 'Ser'
!	Text	!fs	all entries not containing 'fs'
^	Text	^p.(Arg	all entries beginning with 'p.(Arg'
$	Text	Ser)$	all entries ending with 'Ser)'
=""	Text	=""	all entries with this field empty
=""	Text	="p.0"	all entries exactly matching 'p.0'
!=""	Text	!=""	all entries with this field not empty
!=""	Text	!="p.0"	all entries not exactly matching 'p.0?'
combination	Text	*\|Ter !fs	all entries containing '*' or 'Ter' but not containing 'fs'
	Date	2020	all entries matching the year 2020
\|	Date	2020-03\|2020-04	all entries matching March or April, 2020
!	Date	!2020-03	all entries not matching March, 2020
<	Date	<2020	all entries before the year 2020
<=	Date	<=2020-06	all entries in or before June, 2020
>	Date	>2020-06	all entries after June, 2020
>=	Date	>=2020-06-15	all entries on or after June 15th, 2020
combination	Date	2019\|2020 <2020-03	all entries in 2019 or 2020, and before March, 2020
	Numeric	23	all entries exactly matching 23
\|	Numeric	23\|24	all entries exactly matching 23 or 24
!	Numeric	!23	all entries not exactly matching 23
<	Numeric	<23	all entries lower than 23
<=	Numeric	<=23	all entries lower than, or equal to, 23
>	Numeric	>23	all entries higher than 23
>=	Numeric	>=23	all entries higher than, or equal to, 23
combination	Numeric	>=20 <30 !23	all entries with values from 20 to 29, but not equal to 23

Some more advanced examples:

Example	Matches
Asian	all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian	all entries containing 'Asian' but not containing 'Caucasian'
Asian\|African !Caucasian	all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"	all entries containing 'South Asian', but not containing 'South East Asian'

To sort on a certain column, click on the column header or on the arrows. If that column is already selected to sort on, the sort order will be swapped. The column currently sorted on has a darker blue background color than the other columns. The up and down arrows next to the column name indicate the current sorting direction. When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.

73 entries on 1 page. Showing entries 1 - 73.

Legend

How to query

Individual ID	ID_report	Reference	Remarks	Gender	Consanguinity	Country	Population	Age at death	VIP	Data_av	Treatment	Disease	Phenotype details	Variants	Panel size	Owner
00060208	Pat9bl	PubMed: Neveling 2013	-	-	-	-	-	-	-	-	-	RP	-	1	1	Marcel Nelen
00060209	Pat10bl	PubMed: Neveling 2013	-	-	-	-	-	-	-	-	-	RP	-	1	1	Marcel Nelen
00100098	PKRD176;61176	PubMed: Maranha 2015, Journal: Maranhao 2015, PubMed: Li 2017	-	M	yes	Pakistan	Pakistani	-	-	-	-	retinal disease	-	1	1	James Hejtmancik
00291822	-	PubMed: Narang 2020, Journal: Narang 2020	analysis 2794 individuals (India)	-	-	India	-	-	-	-	-	?	-	1	2	Mohammed Faruq
00324157	Fam151Pat18	PubMed: Balciuniene 1995, PubMed: Reinis 2012	5-generation family, 22 affected	M	-	Sweden	-	>12y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551)	1	22	Mariah De Bruin
00324158	Fam151Pat17	PubMed: Reinis 2012	-	M	-	Sweden	-	>25y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551)	1	1	Mariah De Bruin
00324159	Fam151Pat16	PubMed: Reinis 2012	-	M	-	Sweden	-	>35y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551)	1	1	Mariah De Bruin
00324160	Fam151Pat15	PubMed: Reinis 2012	-	F	-	Sweden	-	>26y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551)	1	1	Mariah De Bruin
00324161	Fam151Pat14	PubMed: Reinis 2012	-	F	-	Sweden	-	>32y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551)	1	1	Mariah De Bruin
00324162	Fam151Pat13	PubMed: Reinis 2012	-	F	-	Sweden	-	>32y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551)	1	1	Mariah De Bruin
00324163	Fam151Pat12	PubMed: Reinis 2012	-	F	-	Sweden	-	>46y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551)	1	1	Mariah De Bruin
00324164	Fam151Pat11	PubMed: Reinis 2012	-	M	-	Sweden	-	>32y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551)	1	1	Mariah De Bruin
00324165	Fam151Pat10	PubMed: Reinis 2012	-	M	-	Sweden	-	>27y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551)	1	1	Mariah De Bruin
00324166	Fam151Pat9	PubMed: Reinis 2012	-	F	-	Sweden	-	>44y	-	-	-	CORD5	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551)	1	1	Mariah De Bruin
00324300	Fam151Pat8	PubMed: Reinis 2012	-	M	-	Sweden	-	>53y	-	-	-	CORD5	color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324301	Fam151Pat7	PubMed: Reinis 2012	-	F	-	Sweden	-	>72y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324302	Fam151Pat6	PubMed: Reinis 2012	-	M	-	Sweden	-	>51y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324303	Fam151Pat5	PubMed: Reinis 2012	-	F	-	Sweden	-	>60y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324304	Fam151Pat4	PubMed: Reinis 2012	-	F	-	Sweden	-	>64y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324305	Fam151Pat3	PubMed: Reinis 2012	-	M	-	Sweden	-	>69y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324306	Fam151Pat2	PubMed: Reinis 2012	-	F	-	Sweden	-	>71y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324307	Fam151Pat1	PubMed: Reinis 2012	-	F	-	Sweden	-	>75y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324326	Fam152Pat17	PubMed: Reinis 2012	7-generation family, 17 affected	F	-	Sweden	-	>21y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	17	Mariah De Bruin
00324327	Fam152Pat16	PubMed: Reinis 2012	-	M	-	Sweden	-	>17y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324328	Fam152Pat15	PubMed: Reinis 2012	-	F	-	Sweden	-	>22y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324329	Fam152Pat14	PubMed: Reinis 2012	-	M	-	Sweden	-	>08y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324330	Fam152Pat13	PubMed: Reinis 2012	-	M	-	Sweden	-	>32y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324331	Fam152Pat12	PubMed: Reinis 2012	-	M	-	Sweden	-	>35y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324332	Fam152Pat11	PubMed: Reinis 2012	-	F	-	Sweden	-	>28y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324333	Fam152Pat10	PubMed: Reinis 2012	-	F	-	Sweden	-	>36y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324334	Fam152Pat9	PubMed: Reinis 2012	-	F	-	Sweden	-	>23y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324335	Fam152Pat8	PubMed: Reinis 2012	-	F	-	Sweden	-	>44y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324336	Fam152Pat7	PubMed: Reinis 2012	-	F	-	Sweden	-	>56y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324337	Fam152Pat6	PubMed: Reinis 2012	-	F	-	Sweden	-	>56y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324387	Fam152Pat5	PubMed: Reinis 2012	-	F	-	Sweden	-	>60y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324388	Fam152Pat4	PubMed: Reinis 2012	-	F	-	Sweden	-	>59y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324389	Fam152Pat3	PubMed: Reinis 2012	-	F	-	Sweden	-	>61y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324390	Fam152Pat2	PubMed: Reinis 2012	-	F	-	Sweden	-	>63y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324391	Fam152Pat1	PubMed: Reinis 2012	-	F	-	Sweden	-	>66y	-	-	-	CORD5	Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608	1	1	Mariah De Bruin
00324392	AVM306	PubMed: Wang 2013	2-generation family, 1 affected, unaffected non-carrier parents	F	-	China	Han	?	-	-	-	?	cerebral arteriovenous malformation	1	1	Mariah De Bruin
00326806	patient	PubMed: Bakhoum, 2018	-	M	?	United States	-	>85y	-	-	-	retinal disease	see paper; ..., diabetes mellitus type 2, hypertension, benign prostate hyperplasia, 2 episodes of ischemic stroke, decreased vision after cataract surgery with multifocal lens implant	1	1	Mariah De Bruin
00327541	Fam151	PubMed: Köhn 2007	5-generation family, 28 affected (13F, 15M)	F;M	-	Sweden	-	-	-	-	-	retinal disease	see paper; ...	1	28	Johan den Dunnen
00327542	Fam152	PubMed: Köhn 2007	7-generation family, 21 affected (16F, 5M)	F;M	-	Sweden	-	-	-	-	-	retinal disease	see paper; ...	1	21	Johan den Dunnen
00327543	FamUK	PubMed: Köhn 2010	2-generation family, affected mother/daughter	F	-	United Kingdom (Great Britain)	-	-	-	-	-	retinal disease	see paper; ...	1	2	Johan den Dunnen
00327544	FamGer	PubMed: Köhn 2010	patient	-	-	Germany	-	-	-	-	-	retinal disease	see paper; ...	1	1	Johan den Dunnen
00327545	patient	PubMed: Köhn 2010	-	-	-	United States	-	-	-	-	-	retinal disease	-	1	1	Johan den Dunnen
00327546	patient	PubMed: Köhn 2010	-	-	-	Sweden	-	-	-	-	-	retinal disease	-	1	1	Johan den Dunnen
00333353	Pat9	PubMed: Costa 2017	-	F	-	Brazil	-	-	-	-	-	retinal disease	see paper; ...	1	1	LOVD
00358948	Case71522	PubMed: Tiwari 2016	see paper	M	-	Switzerland	-	-	-	-	-	retinal disease	see paper; ...	1	1	LOVD
00359333	32296	PubMed: Khan 2017	see paper	-	-	United Kingdom (Great Britain)	-	-	-	-	-	retinal disease	see paper; ...	1	1	LOVD
00373864	Rp278B	PubMed: Zhao 2015	family	-	-	Northern Ireland	-	-	-	-	-	retinal disease	see paper; ...	1	1	LOVD
00374924	S4-1	PubMed: Huang 2015	-	M	-	China	-	-	-	-	-	retinal disease	best corrected visual acuity 0.4/0.5	1	1	LOVD
00375415	RP#007	PubMed: Katagiri 2014	family	-	-	Japan	-	-	-	-	-	retinal disease	see paper; ...	1	1	LOVD
00375428	RP#022	PubMed: Katagiri 2014	family	-	-	Japan	-	-	-	-	-	retinal disease	see paper; ...	1	1	LOVD
00375435	RP#030	PubMed: Katagiri 2014	family	-	-	Japan	-	-	-	-	-	retinal disease	see paper; ...	1	1	LOVD
00377722	-	PubMed: Bowne 2011	-	-	no	-	white	-	-	-	-	retinal disease	-	1	1	LOVD
00379651	IR_GS_0033	-	-	M	-	Korea, South (Republic)	-	-	-	-	-	STGD	HP:0032037, HP:0001129, HP:0000006, HP:0000548	1	1	Jinu Han
00381173	-	PubMed: Neveling-2013	-	-	-	-	-	-	-	-	-	retinal disease	-	1	1	Julia Lopez
00381174	-	PubMed: Neveling-2013	-	-	-	-	-	-	-	-	-	retinal disease	-	1	1	Julia Lopez
00381808	-	PubMed: Wang-2014	-	-	-	-	-	-	-	-	-	retinal disease	-	1	1	LOVD
00382575	437	PubMed: Jespersgaar 2019	-	?	-	Denmark	-	-	-	-	-	retinal disease	-	1	1	LOVD
00382576	438	PubMed: Jespersgaar 2019	-	?	-	Denmark	-	-	-	-	-	retinal disease	-	1	1	LOVD
00382577	439	PubMed: Jespersgaar 2019	-	?	-	Denmark	-	-	-	-	-	retinal disease	-	1	1	LOVD
00385417	F28-II-3	PubMed: Chen 2020	-	M	-	Taiwan	-	-	-	-	-	retinal disease	48	1	1	LOVD
00386198	RPN-317	PubMed: Rodriguez-Munoz 2020	family fRPN-153, proband	F	-	Spain	-	-	-	-	-	retinal disease	-	1	1	LOVD
00386222	RPN-363	PubMed: Rodriguez-Munoz 2020	family fRPN-178, proband	M	-	Spain	-	-	-	-	-	retinal disease	-	1	1	LOVD
00386228	RPN-407	PubMed: Rodriguez-Munoz 2020	-	?	-	Spain	-	-	-	-	-	retinal disease	-	1	1	LOVD
00386253	RPN-520	PubMed: Rodriguez-Munoz 2020	-	?	-	Spain	-	-	-	-	-	retinal disease	-	1	1	LOVD
00389733	1017	PubMed: Weisschuh 2020	Filing key number: 491, cone dystrophy, no patient Ids, consecutive numbers given	M	-	Germany	-	-	-	-	-	retinal disease	age at genetic diagnosis mentioned	1	1	LOVD
00447011	ARRP-477	PubMed: Weisschuh 2024	family, 3 affected	M	-	Germany	-	-	-	-	-	?	-	1	3	Johan den Dunnen
00447501	ARRP-426	PubMed: Weisschuh 2024	family, 2 affected	F	-	Germany	-	-	-	-	-	?	-	1	2	Johan den Dunnen
00447577	OAK-717	PubMed: Weisschuh 2024	family, 2 affected	M	-	Germany	-	-	-	-	-	?	-	1	2	Johan den Dunnen
00447723	UD-103	PubMed: Weisschuh 2024	patient, no family history	F	-	Germany	-	-	-	-	-	?	-	1	1	Johan den Dunnen

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Global Variome shared LOVD

PITPNM3 (PITPNM family member 3)