Global Variome shared LOVD
C8orf37 (chromosome 8 open reading frame 37)
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Curator:
Kornelia Neveling
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Phenotypes for disease #00302 (ACLS;JBTS12 (acrocallosal syndrome; (ACLS, Joubert syndrome, type 12 (JBTS-12))), OMIM:200990)
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.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
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
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
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
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
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
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
Protein
: result from protein staining
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Text
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combination
Text
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Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
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all entries not matching March, 2020
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Date
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all entries before the year 2020
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Date
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all entries in or before June, 2020
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Date
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all entries after June, 2020
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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
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Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
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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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9 entries on 1 page. Showing entries 1 - 9.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000002977
Vermis: molar tooth sign; Corpus callosum: agenesis; Lower limb polydactyly: preaxial right; Mental retardation, facial dysmorphism
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004260
0000002978
Vermis: molar tooth sign; Corpus callosum: agenesis; Temporal pachygyria, malformed hippocampus; Upper limb polydactyly: postaxial right and left; Mental retardation, macrocephaly, large fontanelle, depressed and wide nasal bridge, short philtrum, bilateral optic atrophy, ventricular septal defect
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004261
0000002979
Vermis: molar tooth sign; Corpus callosum: agenesis; Wide ventricles; Upper limb polydactyly: postaxial right and left; Lower limb polydactyly: postaxial right and left; Mental retardation, hypotonia, macrocephaly, prominent forehead, hypertelorism, wide nasal bridge, short philtrum, high palate, nail dystrophy
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004262
0000002980
Vermis: molar tooth sign; Corpus callosum: thin; Wide ventricles, hypomyelinization; Upper limb polydactyly: cutaneous syndactyly; Lower limb polydactyly: postaxial right and left, cutaneous syndactyly; Mental retardation, hypotonia, macrocephaly, prominent forehead, hypertelorism, depressed and wide nasal bridge, short philtrum, congenital hypothryroidism
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004263
0000002981
Corpus callosum: agenesis; Wide ventricles, poor frontal cortical development; Upper limb polydactyly: postaxial right and left; Lower limb polydactyly: preaxial and postaxial right and left; Mental retardation, macrocephaly, frontal bossing, hypertelorism, broad nasal bridge, notched nasal tip, low-set ears
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004264
0000002982
Corpus callosum: agenesis; Upper limb polydactyly: postaxial right and left; Lower limb polydactyly: postaxial right and left; Mental retardation, macrocephaly, broad forehead, hypertelorism, peri-orbital fullness, wide nasal bridge, high palate, micrognathia
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004265
0000002983
Vermis: molar tooth sign; Corpus callosum: thin?; Para-callosal cyst; lower limb polydactyly: preaxial; Mental retardation, hypertelorism, dental anomalies (teeth loss, implantation anomalies), retrognatism
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004266
0000002984
Vermis: molar tooth sign; Corpus callosum: agenesis; Upper limb polydactyly: postaxial left; Lower limb polydactyly: preaxial; Cleft palate; Mental retardation, macrocephaly, hypertelorism
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004267
0000002988
-
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004271
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