Global Variome shared LOVD
OPN1MW (opsin 1 (cone pigments), medium-wave-sensitive)
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Phenotypes for disease #02323 (FANCE (Fanconi anemia, complementation group E (FANCE)), OMIM:600901)
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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all entries matching the year 2020
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Date
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20 entries on 1 page. Showing entries 1 - 20.
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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
0000018001
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020230
0000018002
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020231
0000018003
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020232
0000018004
-
-
-
Unknown
-
-
-
-
-
Johan de Winter
00020233
0000018005
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020234
0000018006
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020235
0000018021
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020250
0000018022
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020251
0000018023
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020252
0000018024
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020253
0000018025
-
-
-
Unknown
-
-
-
-
-
Johan de Winter
00020254
0000018026
-
-
-
Unknown
-
-
-
-
-
Johan de Winter
00020255
0000018027
-
-
-
Unknown
-
-
-
-
-
Johan de Winter
00020256
0000018028
-
-
-
Unknown
-
-
-
-
-
Johan de Winter
00020257
0000018029
-
-
-
Unknown
-
-
-
-
-
Johan de Winter
00020258
0000018030
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020259
0000018031
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020260
0000018032
-
-
-
Unknown
-
-
-
-
-
Arleen D. Auerbach
00020261
0000018033
-
-
-
Unknown
-
-
-
-
-
Johan de Winter
00020262
0000322445
Abnormality of prenatal development or birth, Intrauterine growth retardation, Aplasia/hypoplasia involving bones of the upper limbs, Microcephaly
prenatal
-
Unknown
19+5
-
-
-
-
Andreas Laner
00431877
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