Global Variome shared LOVD
SEMA3E (sema domain, immunoglobulin domain (Ig), sh...)
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Phenotypes for disease #01611 (DDS (Denys-Drash syndrome (DDS)), OMIM:194080)
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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Text
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space
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Text
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Text
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all entries beginning with 'p.(Arg'
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Text
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Text
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Text
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combination
Text
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Date
2020
all entries matching the year 2020
|
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
>
Date
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all entries after June, 2020
>=
Date
>=2020-06-15
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
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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'
Asian|African !Caucasian
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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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
0000152706
Son, 46, XY, ambiguous genitalia and ventricular septal defect. Laparoscopy performed at 1 year for undescended testes - bilateral fallopian tubes and right fimbriae, no uterus, left gonad looked like a testicle, right one like an ova-testis. No Wilms tumor at 6 years of age.
-
-
Familial
-
1y
-
-
-
Olga Beltcheva
00204202
0000152715
Renal biopsy
-
-
Isolated (sporadic)
-
-
4m24d
-
-
Olga Beltcheva
00204211
0000152716
Male (XY) with female genitalia with clitoromegaly, labial fusion. Gonadal hystology demonstrates the presence of testes.
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204212
0000152717
Male - 46XY, cryptorchidism, perineal hypospadias, Wilms tumour and diffuse mesangial sclerosis
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204213
0000152718
46XY patient with nephropathy and gonadoblastoma
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204214
0000152719
DMS
-
-
Isolated (sporadic)
-
-
1y3m18d
-
-
LOVD
00204215
0000152720
46 XY patient woth ambiguous genitalia, Wilms tumor and gondaoblastoma
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204216
0000152721
Male patient (46,XY) born with normal external female genitalia, presented with nephroticsyndrome.
-
-
Unknown
-
-
6m
nephrotic syndrome
-
Olga Beltcheva
00204217
0000152722
Ambiguous genitalia, nephropathy
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204218
0000152723
46 XY, Ambiguou genitalia, Wilms tumor, gonadoblastoma
-
-
Isolated (sporadic)
-
-
-
-
-
Olga Beltcheva
00204219
0000152724
Nephropathy, bilateral Wilms tumor
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204220
0000152725
46XY patient with ambiguous, nepropathy, bilateral Wilms tumor
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204221
0000152726
46XX patient with nepropathy and Wilms tumor
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204222
0000152727
46XX patient with nepropathy and Wilms tumor
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204223
0000152728
46XY patient with ambiguous genitalia, nepropathy and Wilms tumor
-
-
Unknown
-
-
-
-
-
Olga Beltcheva
00204224
0000152730
46XX patient with nephropathy
-
-
Isolated (sporadic)
-
-
-
-
-
Olga Beltcheva
00204226
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