Disease #00336 (ARCND1 (auriculocondylar syndrome, type 1 (ARCND-1)), OMIM:602483)

Official abbreviation	ARCND1
Name	auriculocondylar syndrome, type 1 (ARCND-1)
OMIM ID	602483
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	7
Phenotype entries for this disease	6
Associated with 1 gene	GNAI3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-02-24 22:57:33 +01:00 (CET)
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
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Albania
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Algeria
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Bulgaria
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Cambodia
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Cameroon
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Canada
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Central Europe
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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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Germany
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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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Laos
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Latvia
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Lesotho
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Liberia
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Libya
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Lithuania
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Malawi
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Peru
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Romania
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Russia
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Russian Federation
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Scotland
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Singapore
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Spain
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St. Helena, Ascension and Tristan da
Cunha
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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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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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Vanuatu
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Viet Nam
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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
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Yemen
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Yugoslavia
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Zaire
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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
	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'

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7 entries on 1 page. Showing entries 1 - 7.

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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
00016105	-	PubMed: Erlich 2000, PubMed: Rieder 2012	2-generation family, daugther (affected mother S012-P)	F	no	-	-	-	-	-	-	ARCND1	severe mandibular abnormalities, congenital mandibular ankylosis with lateral fusion mandible to temporozygomatic suture, medial fusion to skull base (medial and lateral pterygoid plates), resulting in airway obstruction requiring tracheostomy; severe microglossia, elongated soft-tissue masses attached at posterior floor mouth, excessive soft tissue protruding from medial alveolus lower jaw	DLX5, DLX6, EDNRA, GNAI3	GNAI3	1	2	Johan den Dunnen
00016106	-	PubMed: Rieder 2012	2-generation family, affected mother of S011	F	no	-	-	-	-	-	-	ARCND1	-	GNAI3	GNAI3	1	1	Johan den Dunnen
00016107	-	PubMed: Rieder 2012	2-generation family, affected daugther	F	no	-	-	-	-	-	-	ARCND1	-	GNAI3	GNAI3	1	2	Johan den Dunnen
00016123	-	PubMed: Guion-Almeida 2002; PubMed: Masotti 2008	familial case; except for one non-penetrant individual the variant segregates with the ARCND1 phenotype	-	no	Brazil	-	-	-	-	-	ARCND1	-	GNAI3	GNAI3	1	3	Maria Rita Passos-Bueno
00016124	-	PubMed: Propst 2013	-	M	no	-	-	-	-	-	-	ARCND1	-	GNAI3	GNAI3	1	1	Maria Rita Passos-Bueno
00016125	-	-	-	M	no	-	-	-	-	-	-	ARCND1	-	GNAI3	GNAI3	1	1	Maria Rita Passos-Bueno
00016207	-	PubMed: Gordon 2013	2-generation family, daugther and father (23315542-Pat7f)	F	no	-	-	-	-	-	-	ARCND1	question mark ears, micro- and/or retrognathia, facial asymmetry; presented with asymmetric micrognathia, malocclusion, microstomia, notch between lobe and helix right ear; X-ray mildly hypoplastic first ribs	GNAI3, PLCB4	GNAI3	1	2	Johan den Dunnen

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