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REST (RE1-silencing transcription factor)
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Phenotypes for disease #05727 (NEDVIBA (neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA)), OMIM:618547)
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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.
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
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
How to query this table
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all entries containing 'Arg'
space
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Text
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all entries beginning with 'p.(Arg'
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combination
Text
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Date
2020
all entries matching the year 2020
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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
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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
>=
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'
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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
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Owner
Individual ID
0000301943
-
neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA)
Prenatal development: unremarkable; developmental delay, intellectual disability ; no microcephaly; short stature; age at sitting: delayed; age at walking: 2y3m; age at talking & current speech:delayed; dysmorphic features: 5th finger clinodactyly; neurologic & behavioral problems: ataxia anxiety; electroencephalogram: not available; brain magnetic resonance: abnormal signaling in caudate pathway and putamen; visual abnormalities: retinitis pigmentosa, peripheral vision loss and gaze abnormality; other abnormalities: kyphoscoliosis, pes planus
Isolated (sporadic)
34y
-
-
-
LOVD
00409828
0000301944
-
neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA)
Prenatal development: cystic brain lesions found at 7m gestation but later resolved; developmental delay, intellectual disability ; no microcephaly; short stature; age at sitting: 2y; age at walking: cannot walk unassisted; age at talking & current speech:First words at 14 months & significantly limited, expressive language now, only a few words; dysmorphic features: right earlobe crease, frontal bossing, epicanthal folds, anteverted nose, bulbous nasal tip, preauricular pit, thin upper lip; neurologic & behavioral problems: truncal hypotonia limb hypertonia (lower > upper) brisk deep tendon reflexs some contractures in hamstrings, no self-care skills; electroencephalogram: normal; brain magnetic resonance: cerebral & cerebellar atrophy, thin corpus callosum, periventricular leukomalacia, possible gray matter heterotropia; visual abnormalities: cortical visual impairment, strabismus, astigmatism; other abnormalities: scoliosis, bilateral hip dislocation (Wears AFOs), torticollis, clonus, and spasticity as innt, poor weight gain
Isolated (sporadic)
9y
-
-
-
LOVD
00409829
0000301945
-
neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA)
Prenatal development: unremarkable; developmental delay, intellectual disability ; no microcephaly; no short stature; age at sitting: 8m; age at walking: 1y6m; age at talking & current speech:2 years & Speaks in sentences and has word finding difficulties; dysmorphic features: none; neurologic & behavioral problems: ataxia, staring spells, tingling in legs (electromyography normal), hypotonia, will hug and kiss strangers; electroencephalogram: normal; brain magnetic resonance: cystic lesion on brain; visual abnormalities: retinitis pigmentosa, cone-rod dystrophy, optic atrophy, photophobia, slight exotropia, bilateral strabismus; other abnormalities: familial mediterranean fever (heterozygous MEFV mutation), gags easily and sometimes chokes on f
Isolated (sporadic)
14y
-
-
-
LOVD
00409830
0000301946
-
neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA)
Prenatal development: premature, born at 8m gestation; developmental delay, intellectual disability ; no microcephaly; no short stature; age at sitting: 8m; age at walking: 1y4m; age at talking & current speech:1y6m; dysmorphic features: none; neurologic & behavioral problems: none; electroencephalogram: not available; brain magnetic resonance: not available; visual abnormalities: retinitis pigmentosa (age of diagnosis: 7 years), optic atrophy; other abnormalities: hypertension
Isolated (sporadic)
44y
-
-
-
LOVD
00409831
0000301947
-
neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA)
Prenatal development: unremarkable; developmental delay, intellectual disability ; no microcephaly; no short stature; age at sitting: n/a; age at walking: 1y; age at talking & current speech:delayed & dysarthric speech; dysmorphic features: flat occiput, slight synophrys (father), widely spaced teeth; neurologic & behavioral problems: progressive neurologic decline, abnormal tone, mild wide spaced gait, bulbar weakness (mild drooling), swallowing dysfunction recent onset right-sided facial weakness; electroencephalogram: mild diffuse slowing; brain magnetic resonance: lesions in brainstem (concerning for a demyelinating disease vs autoimmune process vs Guillain Barre syndrome); visual abnormalities: bilateral optic atrophy; other abnormalities: full cheeks (steroid usage) ,truncal obesity, high blood vs zero cerebrospinal fluid glutamine, high cerebrospinal fluid lactate and pyruvate, high peripheral blood lactate
Isolated (sporadic)
8y
-
-
-
LOVD
00409832
0000301948
-
neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA)
Prenatal development: unremarkable; developmental delay, intellectual disability ; no microcephaly; no short stature; age at sitting: not achieved; age at walking: not achieved; age at talking & current speech:not achieved; dysmorphic features: none; neurologic & behavioral problems: seizures infantile spasms limb hypertonia; electroencephalogram: consistent with early myoclonic epileptic encephalopathy; brain magnetic resonance: abnormal autopsy findings volume loss along the white matter adjacent to the atria and frontal horns of the ventricle, atrophy of pons and brainstem, bilateral subdural fluid collection; visual abnormalities: optic atrophy nystagmus; other abnormalities: feeding difficulty, gastroesophageal reflux disease, small umbilical hernia, laryngotracheomalacia
Isolated (sporadic)
<1y
-
-
-
LOVD
00409833
0000301949
-
neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA)
Prenatal development: unremarkable; developmental delay, intellectual disability ; no microcephaly; no short stature; age at sitting: not achieved; age at walking: not achieved; age at talking & current speech:not achieved; dysmorphic features: none; neurologic & behavioral problems: seizures infantile spasms hypertonia; electroencephalogram: abnormal (verbal disclosure); brain magnetic resonance: ventricular dilatation predominantly involving the occipital and temporal horns of the lateral ventricles with prominence of the subarachnoid space raising the possibility of underlying atrophy and a migrational anomaly; visual abnormalities: optic atrophy; other abnormalities: failure to thrive, gastroesophageal reflux disease, g-tube, hearing loss, laryngotracheomalacia respiratory distress
Isolated (sporadic)
<1y
-
-
-
LOVD
00409834
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