Global Variome shared LOVD
VAMP1 (vesicle-associated membrane protein 1 (syna...))
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Phenotypes for disease #04282 (CVI (cerebral visual impairment (CVI)))
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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all entries in 2019 or 2020, and before March, 2020
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Numeric
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all entries exactly matching 23 or 24
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27 entries on 1 page. Showing entries 1 - 27.
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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
0000034039
Tapered finger (HP:0001182); Abnormal finger flexion creases (HP:0006143); 2-3 toe syndactyly (HP:0004691); Feeding difficulties in infancy (HP:0008872); Reduced visual acuity (HP:0007663); Strabismus (HP:0000486); Nystagmus (HP:0000639); Cataract (HP:0000518); Optic atrophy (HP:0000648); Cerebral visual impairment (HP:0100704); Intellectual disability, mild (HP:0001256)
-
-
Isolated (sporadic)
24y
-
-
-
-
Marc Ferre
00043810
0000034040
Prominent nasal bridge (HP:0000426); Prominent antihelix (HP:0000395); Clinodactyly of the 5th finger (HP:0004209); Feeding difficulties in infancy (HP:0008872); Reduced visual acuity (HP:0007663); Strabismus (HP:0000486); Abnormality of eye movement (HP:0000496); Nystagmus (HP:0000639); Visual field defect (HP:0001123); Optic atrophy (HP:0000648); Neurodevelopmental delay (HP:0012758);Cerebral visual impairment (HP:0100704)
-
-
Unknown
04y
-
-
-
-
Marc Ferre
00043811
0000034041
birth 39w, weight 3640g; height 118cm (P50), OFC 51,5cm (P40); delayed motor mevelopment; normal language development; intellectual disability; autism; normal muscle tone; no epilepsy; MRI normal; nystagmus; normal hearing; long eyelashes; full nasal tip, long columella; thin upper lip; large ears; joint laxity; fragmented palmar creases, short distal finger and toe phalanges, longitudinally grooved fingernails, fetal finger pads, syndactyly II-III toes, clinodactyly IV-V toes
-
MRD62
Isolated (sporadic)
05y
-
-
-
-
Johan den Dunnen
00039389
0000034042
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039390
0000034043
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039391
0000034044
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039392
0000034045
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039393
0000034046
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039394
0000034047
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039395
0000078830
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039396
0000078831
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039397
0000078832
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039402
0000078833
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039401
0000078834
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039398
0000078835
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039399
0000078836
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039403
0000078837
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039404
0000078838
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039405
0000078839
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039406
0000078840
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039412
0000078841
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00025011
0000078842
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039407
0000078843
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039408
0000078844
see paper; ..., no intrauterine growth retardation; intellectual disability/developmental delay/autism; seizures; no hypotonia; no behavioral problems; no spastic quadriparesis; no ttention deficit hyperactivity disorder; feeding/swallowing problems; thin corpus callosum; diminished white matter volume; abnormal cerebellar vermis; ventriculomegaly; no small pons; no abnormal hippocampus; no small anterior commissure; no delayed myelination; no coloboma; optic nerve atrophy/hypoplasia; no microphthalmia; no Peter’s anomaly; no iris anomalies; blepharophimosis; no sensorineural hearing loss; no choanal atresia; no cleft lip; no ventricular septal defect; no patent foramen ovale; no patent ductus arteriosus; no anomalous pulmonary venous return; gastroesophageal reflux disease; no duodenal atresia; no annular pancreas; pyloric hypertrophy; vesicoureteral reflux; no cystic kidney; no hypospadias; no cryptorchidism; no syndactyly; no hip dysplasia; no scoliosis; no lumbar lordosis; tall stature (≥98th centile); no short stature (≤2nd centile); no macrocephaly (≥98th centile); no microcephaly (≤2nd centile); no third fontanel; frontal bossing; no triangular face; no abnormal eyebrows; no hypotelorism; no hypertelorism; no upslanting palpebral fissures; no down-slanting palpebral fissures; no small palpebral fissures; no epicanthal folds; deeply set eyes; blepharaophymosis; abnormal ears; no preauricular pits; bulbous nose; no anteverted nares; no flat philtrum; full lips; no small mouth; no furrowed tongue; abnormal teeth; broad alveolar ridges; high arched palate; no micrognathia; no small nipples; no inverted nipples; no small hands; no syndactyly; no 5th finger clinodactyly; no digital anomalies; no nail hypoplasia; no abnormal palmar creases; no widow’s peak; no sacral hair tuft; no cafe au lait spots
-
NEDBEH
Isolated (sporadic)
12y08m
-
-
-
-
Johan den Dunnen
00039409
0000078845
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00039411
0000337343
Bilaterally increased P100 wave latency with normal amplitude
-
-
Familial, autosomal recessive
-
-
-
-
-
Barbara Vona
00448132
0000337346
Bilateral macular colobomata
-
-
Familial, autosomal recessive
-
-
-
-
-
Barbara Vona
00448134
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