Global Variome shared LOVD
CNBD1 (cyclic nucleotide binding domain containing 1)
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Phenotypes for disease #01723 (ACCPN (agenesis, corpus callosum, with peripheral neuropathy (ACCPN, Andermann syndrome)), OMIM:218000)
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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.
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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19 entries on 1 page. Showing entries 1 - 19.
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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
0000036698
see paper; Andermann syndrome; hypotonia, areflexia lower extremities, reduced deep tendon reflexes iupper extremities with normal tonus, delayed motor milestones; MRI complete agenesis corpus callosum, disseminated white matter hyperintensities
-
-
Isolated (sporadic)
07y
-
-
-
-
Johan den Dunnen
00050080
0000036699
see paper; Andermann syndrome; hypotonia, areflexia upper/lower extremities, delayed motor milestones mental retardation, afebrile seizures, dysmorphic features; MRI complete agenesis corpus callosum, batwing appearance frontal horns, enlargement cisterna magna
-
-
Isolated (sporadic)
05y
-
-
-
-
Johan den Dunnen
00050081
0000036701
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00050083
0000036702
see paper; mild Andermann syndrome, ...
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00050084
0000036703
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00050085
0000036704
see paper; feeding difficulties, hypotonia, areflexia upper/lower extremities, delayed motor milestones, mental retardation, seizures, mild dysmorphic feature complete; MRI agenesis of the corpus callosum, enlargement lateral ventricles, deformation gyrus cinguli
-
-
Isolated (sporadic)
01y
-
00y00m13d
-
-
Johan den Dunnen
00050086
0000036705
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00050087
0000036706
motor and sensory neuropathy and corpus callosum agenesis
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00050088
0000036707
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00050089
0000036708
motor and sensory neuropathy and corpus callosum agenesis
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00050090
0000036709
motor and sensory neuropathy and corpus callosum agenesis
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00050092
0000036710
motor and sensory neuropathy and corpus callosum agenesis
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00050093
0000036711
motor and sensory neuropathy and corpus callosum agenesis
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00050094
0000036712
motor and sensory neuropathy and corpus callosum agenesis
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00050095
0000036713
motor and sensory neuropathy and corpus callosum agenesis
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00050096
0000036714
Andermann syndrome
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00037091
0000156809
Andermann syndrome, arthrogryposis
Andermann syndrome, arthrogryposis
-
Unknown
-
-
-
-
-
Andreas Laner
00037087
0000156810
Andermann syndrome, arthrogryposis
Andermann syndrome, arthrogryposis
-
Unknown
-
-
-
-
-
Andreas Laner
00037093
0000156811
Andermann syndrome, arthrogryposis
Andermann syndrome, arthrogryposis
-
Unknown
-
-
-
-
-
Andreas Laner
00037095
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