Disease #04328 (BAIDCS (structural brain anomalies with impaired intellectual development and craniosynostosis (BAIDCS)), OMIM:618736)

Official abbreviation	BAIDCS
Name	structural brain anomalies with impaired intellectual development and craniosynostosis (BAIDCS)
OMIM ID	618736
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	5
Phenotype entries for this disease	5
Associated with 1 gene	ZIC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-12 21:00:16 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Individuals

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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
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Algeria
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Andorra
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Angola
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Brazil
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British Indian Ocean Territory
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Brunei Darussalam
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Bulgaria
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Burkina Faso
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Burundi
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Cambodia
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Cameroon
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Canada
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Cape Verde
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Cayman Islands
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Central African Republic
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Central Europe
Chad
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Chile
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China
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Christmas Island
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Cocos (Keeling Islands)
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Colombia
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Comoros
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Congo
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Cook Islands
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Costa Rica
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Cote D'Ivoire (Ivory Coast)
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Croatia (Hrvatska)
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Cuba
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Cyprus
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Estonia
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Ethiopia
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Faroe Islands
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Fiji
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Finland
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France
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Gabon
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Gambia
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Georgia
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Germany
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Ghana
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Gibraltar
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Guatemala
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Guinea
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Guyana
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Italy
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Japan
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Jordan
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Kenya
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Kiribati
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Korea
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Korea, North (People's Republic)
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Korea, South (Republic)
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Kosovo
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Kuwait
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Kyrgyzstan (Kyrgyz Republic)
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Laos
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Latvia
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Lebanon
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Lesotho
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Liberia
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Libya
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Liechtenstein
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Lithuania
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Luxembourg
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Macedonia
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Madagascar
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Malawi
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Malaysia
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Panama
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Peru
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Romania
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Russia
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San Marino
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Saudi Arabia
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Scotland
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Serbia
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Singapore
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Slovakia (Slovak Republic)
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Slovenia
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Soviet Union (former)
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Spain
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St. Helena, Ascension and Tristan da
Cunha
(St. Helena, Ascension and Tristan da
Cunha)
St. Pierre and Miquelon
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Sudan
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Sudan, South
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Suriname
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Swaziland
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Sweden
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Switzerland
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Syria
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Taiwan
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Tajikistan
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Tanzania
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Thailand
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Togo
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Tokelau
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Tonga
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Trinidad and Tobago
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Tunisia
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Turkey
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Turkmenistan
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Turks and Caicos Islands
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Tuvalu
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Uganda
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Ukraine
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United Arab Emirates
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United Kingdom (Great Britain)
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United States
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Uruguay
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US Minor Outlying Islands
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Uzbekistan
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Vanuatu
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Venezuela
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Viet Nam
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Virgin Islands (British)
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Virgin Islands (US)
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Wales
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Wallis and Futuna Islands
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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

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Operator	Column type	Example	Matches
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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'

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5 entries on 1 page. Showing entries 1 - 5.

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How to query

Individual ID	ID_report	Reference	Remarks	Gender	Consanguinity	Country	Population	Age at death	VIP	Data_av	Treatment	Disease	Phenotype details	Genes screened	Variants in genes	Variants	Panel size	Owner
00049839	-	PubMed: Twigg 2015, Journal: Twigg 2015	3-generation family, 6 affecteds (2F, 4M)	F	no	United Kingdom (Great Britain)	-	-	-	-	-	BAIDCS	brachycephaly, delayed closure, anterior fontanelle, atrophy rostral part cerebellum and pons, no strabismus/ptosis, mild learning disability	ZIC1	ZIC1	1	5	Johan den Dunnen
00049840	-	PubMed: Twigg 2015, Journal: Twigg 2015	-	M	?	United Kingdom (Great Britain)	-	-	-	-	-	BAIDCS	bicoronal synostosis, 3 craniofacial procedures; MRI abnormal configuration ventricules corpus callosum, moderate/severe learning disability, scoliosis, foreskin stricture	ZIC1	ZIC1	1	1	Johan den Dunnen
00049841	-	PubMed: Twigg 2015, Journal: Twigg 2015	-	F	?	United Kingdom (Great Britain)	-	-	-	-	-	BAIDCS	bicoronal synostosis, severe brachycephaly; MRI agenesis corpus callosum, dilated lateral ventricules; divergent strabismus, moderate learning disability, scoliosis	ZIC1	ZIC1	1	1	Johan den Dunnen
00049842	-	PubMed: Twigg 2015, Journal: Twigg 2015	-	M	-	United Kingdom (Great Britain)	-	-	-	-	-	BAIDCS	bicoronal synostosis, severe brachycephaly, bony defect sagittal suture; CT-scan normal brain; mild learning disability, scoliosis	ZIC1	ZIC1	1	1	Johan den Dunnen
00049843	-	PubMed: Twigg 2015, Journal: Twigg 2015	-	M	-	Netherlands	-	-	-	-	-	BAIDCS	bicoronal synostosis, partial R lambdoid synostosis, bony defect of metopic and sagittal sutures; MRI mildly enlarged lateral ventricles, shortened corpus callosum, hypoplastic pons, enlarged foramen magnum; strabismus sursoadductorius, moderate-severe learning disability	ZIC1	ZIC1	1	1	Johan den Dunnen

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Global Variome shared LOVD

HPDL (4-hydroxyphenylpyruvate dioxygenase-like)