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Phenotypes for disease #02345 (HYPOC1 (hypocalcemia, autosomal dominant, Bartter syndrome incl. (HYPOC-1)), OMIM:601198)
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
How to query this table
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Operator
Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
Arg Ser
all entries containing 'Arg' and 'Ser'
|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
Text
!=""
all entries with this field not empty
!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
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
<=
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'
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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88 entries on 1 page. Showing entries 1 - 88.
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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
0000153027
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204793
0000153031
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204797
0000153054
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204820
0000153055
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204821
0000153056
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204822
0000153057
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204823
0000153058
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204824
0000153059
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204825
0000153060
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204826
0000153061
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204827
0000153062
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204828
0000153063
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204829
0000153064
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204831
0000153065
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204832
0000153066
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204833
0000153067
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204834
0000153068
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204835
0000153069
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204836
0000153070
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204837
0000153071
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204838
0000153072
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204839
0000153073
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204841
0000153074
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204843
0000153075
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204844
0000153076
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204845
0000153082
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204851
0000153083
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204853
0000153084
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204854
0000153085
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204855
0000153112
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204883
0000153136
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204907
0000153137
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204908
0000153138
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204909
0000153139
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204910
0000153140
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204911
0000153141
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204912
0000153146
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204918
0000153147
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204919
0000153148
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204921
0000153149
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204922
0000153150
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204923
0000153161
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204938
0000153174
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204951
0000153191
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204973
0000153197
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204979
0000153201
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204983
0000153207
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204989
0000153210
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204992
0000153211
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204993
0000153212
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204994
0000153214
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204996
0000153215
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204997
0000153216
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00204998
0000153239
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205022
0000153244
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205028
0000153256
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205043
0000153257
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205045
0000153259
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205047
0000153260
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205048
0000153261
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205049
0000153262
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205050
0000153268
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205056
0000153269
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205057
0000153271
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205059
0000153273
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205061
0000153275
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205065
0000153276
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205067
0000153277
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205068
0000153278
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205070
0000153279
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205071
0000153280
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205073
0000153281
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205074
0000153284
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205077
0000153285
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205078
0000153286
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205079
0000153287
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205080
0000153288
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205081
0000153289
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205082
0000153290
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205083
0000153291
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205084
0000153292
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205085
0000153293
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205086
0000153294
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205089
0000153301
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205100
0000153303
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205102
0000153306
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205105
0000153307
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00205106
0000174761
symptomatic hypoclacemia, manifesting as intermittent tetany and muscle spasm
-
-
Familial, autosomal dominant
-
-
-
-
-
Benjamin Kwan
00234341
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