Global Variome shared LOVD
ZNF346 (zinc finger protein 346)
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Phenotypes for disease #05219 (CFM1;HFM (craniofacial microsomia (Goldenhar syndrome)), OMIM:164210)
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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16 entries on 1 page. Showing entries 1 - 16.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000074230
see paper; ...
-
-
Isolated (sporadic)
-
-
-
-
-
Marie Berenguer
00095942
0000074233
see paper; ...
-
-
Familial, autosomal dominant
-
-
-
-
-
Marie Berenguer
00095943
0000074235
see paper; ...
-
-
Familial, autosomal dominant
-
-
-
-
-
Marie Berenguer
00095955
0000074236
-
-
-
Unknown
-
-
-
-
-
Marie Berenguer
00095945
0000074257
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095983
0000074258
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095984
0000074259
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095985
0000074260
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095986
0000074261
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095987
0000074262
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095988
0000074263
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095989
0000074264
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095990
0000074265
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095991
0000074266
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095992
0000074267
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095993
0000074268
oculo-auriculo-vertebral spectrum (OAVS)
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00095994
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