Global Variome shared LOVD
WARS (tryptophanyl-tRNA synthetase)
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Phenotypes for disease #00307 (HYDRO (hydrocephaly (HYDRO)))
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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Date
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Date
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Date
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Date
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Date
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Numeric
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all entries exactly matching 23 or 24
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Numeric
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Numeric
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all entries lower than, or equal to, 23
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Numeric
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Numeric
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all entries with values from 20 to 29, but not equal to 23
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all entries containing 'South Asian', but not containing 'South East Asian'
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16 entries on 1 page. Showing entries 1 - 16.
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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
0000002975
arhinencephaly; Vermis: molar tooth sign; Corpus callosum: absent; Upper limb polydactyly: postaxial right and left; lower limb polydactyly: preaxial right and left; Cleft: palate; hallux duplication; micrognathia
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004258
0000002976
Corpus callosum: ?; hallux duplication
-
-
Unknown
-
-
-
-
-
Tania Attie-Bitach
00004259
0000014802
peripheral neuropathy (demyelinating motor sensory neuropathy ), dysmorphic facial features , hypospadias, craniosynostosis, minor insufficiency of the aortic valve, mild glaucoma, mild learning disabilities
-
-
Familial, autosomal dominant
31y
-
-
-
-
Thomas Potjer
00011647
0000014895
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Thomas Potjer
00016304
0000143365
Hydrocephalus (HP:0000238)
-
-
Familial, X-linked recessive
-
-
-
-
-
Isabel Filges
00181103
0000323839
hydrocephaly; laterality defect; anal imperforation, absence of pulmonary segmentation, cardiopathy, bilobate thymus, unique ombilical artery, enlarged renal bassinet; MRI triventricular hydrocephalus, Sylvius aqueduct stenosis, corpus callosum agenesis hypoplasia of bulbaire pyramids
hydrocephaly
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00433318
0000323840
hydrocephaly (OFC 37cm (+1SD)); MRI pachygyria
hydrocephaly
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00433319
0000323841
hydrocephaly; macrocephaly (OFC 40.5cm (+3SD)); MRI pachygyria
hydrocephaly
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00433320
0000323842
hydrocephaly
hydrocephaly
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00433321
0000323843
hydrocephaly; MRI 22w-H severe, small cerebellum, Sylvius aqueduct agenesis, mild hypoplasia vermis and cerebellum
hydrocephaly
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00433322
0000323844
hydrocephaly
hydrocephaly
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00433323
0000323845
hydrocephaly; MRI Sylvius aqueduct dysplasia, absence of bulbaire pyramids and corpus callosum
hydrocephaly
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00433324
0000323846
hydrocephaly; MRI cerebellum hypoplasia, enlarged lateral ventricles, atrophy of cerebral parenchyma
hydrocephaly
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00433325
0000323847
hydrocephaly
hydrocephaly
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00433326
0000323848
hydrocephaly; pear-shaped head; laterality defect; MRI enlarged lateral ventricles, hemicerebellum hyploplasia, small cerebellum, cortical atrophy, corpus callosum thin and stretched, globally smaller brain, cyst on midline (supra and infra tentoriel), encephalocele
hydrocephaly
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00433327
0000323849
hydrocephaly; severe encephalopathy; severe intellectual deficiency; MRI Sylvius aqueduct stenosis
hydrocephaly
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00433328
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