Global Variome shared LOVD
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
View all genes
Create a new gene entry
View all transcripts
Create a new transcript information entry
View all variants
View all variants affecting transcripts
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
Create a new disease information entry
View available phenotype columns
View all screenings
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
Phenotypes for disease #01462 (CMYO2A;NEM3 (myopathy, congenital, type 2A, typical), OMIM:161800)
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
All list views have search fields which can be used to search data. You can search for a complete word or you can search for a part of a search term. If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify. Note that search terms are case-insensitive and that wildcards such as * are treated as normal text! For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.
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'
To sort on a certain column, click on the column header or on the arrows. If that column is already selected to sort on, the sort order will be swapped. The column currently sorted on has a darker blue background color than the other columns. The up and down arrows next to the column name indicate the current sorting direction. When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.
200 entries on 2 pages. Showing entries 1 - 100.
10 per page
25 per page
50 per page
100 per page
Legend
How to query
« First
Prev
1
2
Next
Last »
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000083983
severe
-
-
Isolated (sporadic)
18m
-
-
-
-
Alan Beggs
00106168
0000083984
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106169
0000083985
typical
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106170
0000083986
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106171
0000083990
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106175
0000083991
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106176
0000083992
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106177
0000083993
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Kristen Nowak
00106178
0000083994
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Kristen Nowak
00106179
0000083995
severe
-
-
Isolated (sporadic)
15d
-
-
-
-
Alan Beggs
00106180
0000083996
somatic mosaicism mother
-
-
Familial, autosomal dominant
-
-
-
-
-
Kristen Nowak
00106181
0000083997
severe; required mechanical ventilation from birth, possibly affected cousin
-
-
Familial, autosomal recessive
22m
-
-
-
-
Kristen Nowak
00106182
0000083998
intranuclear rods
-
-
Isolated (sporadic)
2m
-
-
-
-
Alan Beggs
00106183
0000083999
one intranuclear rod
-
-
Isolated (sporadic)
42y
-
-
-
-
Kristen Nowak
00106184
0000084000
typical
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106185
0000084001
typical, age onset 21y/54y
-
-
Familial, autosomal dominant
-
-
-
-
-
Alan Beggs
00106186
0000084002
mild
-
-
Familial, autosomal dominant
47y
-
-
-
-
Kristen Nowak
00106187
0000084003
-
-
-
Isolated (sporadic)
2m15d
-
-
-
-
Kristen Nowak
00106188
0000084004
severe/intermediate ; Disease severity in email from Norma 2.2.04.
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106189
0000084006
typical, intranuclear rods
-
-
Isolated (sporadic)
8y
-
-
-
-
Kristen Nowak
00106191
0000084007
typical, age onset 7y/48y
-
-
Isolated (sporadic)
-
-
-
-
-
Alan Beggs
00106192
0000084008
severe myopathy, nemaline, type 3 (NEM-3);AM
-
-
Isolated (sporadic)
4m15d
-
-
-
-
Kristen Nowak
00106193
0000084009
severe
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106194
0000084010
severe
-
-
Isolated (sporadic)
5d
-
-
-
-
Alan Beggs
00106195
0000084011
intermediate
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106196
0000084012
severe; no spontaneous movement or respiratory effort at birth; ventilator dependent
-
-
Isolated (sporadic)
1y9m
-
-
-
-
Alan Beggs
00106197
0000084013
severe
-
-
Isolated (sporadic)
10m
-
-
-
-
Kristen Nowak
00106198
0000084014
typical
-
-
Isolated (sporadic)
4y
-
-
-
-
Alan Beggs
00106199
0000084016
typical; 3y-wheelchair bound; both patients hypotonic in first months of life
-
-
Isolated (sporadic)
3y
-
-
-
-
Alan Beggs
00106201
0000084017
severe
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106202
0000084018
severe
-
-
Familial, autosomal recessive
5d
-
-
-
-
Kristen Nowak
00106203
0000084019
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106204
0000084021
arthrogryposis, contractures
-
-
Isolated (sporadic)
<1d
-
-
-
-
Kristen Nowak
00106206
0000084022
severe
-
-
Unknown
5m
-
-
-
-
Kristen Nowak
00106207
0000084024
typical
-
-
Familial, autosomal dominant
35y
-
-
-
-
Kristen Nowak
00106209
0000084025
mild
-
-
Familial, autosomal dominant
42y
-
-
-
-
Kristen Nowak
00106210
0000084026
mild
-
-
Isolated (sporadic)
31y
-
-
-
-
Kristen Nowak
00106211
0000084027
severe
-
-
Isolated (sporadic)
1d
-
-
-
-
Kristen Nowak
00106212
0000084028
mild
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106213
0000084029
severe
-
-
Familial, autosomal recessive
-
-
-
-
-
Kristen Nowak
00106214
0000084030
mild
-
-
Unknown
39y
-
-
-
-
Kristen Nowak
00106215
0000084031
mild
-
-
Unknown
9y
-
-
-
-
Kristen Nowak
00106216
0000084032
typical; no parental DNA
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106217
0000084033
typical
-
-
Familial, autosomal dominant
3y
-
-
-
-
Alan Beggs
00106218
0000084034
typical
-
-
Unknown
45y
-
-
-
-
Kristen Nowak
00106219
0000084036
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106221
0000084038
intranuclear rods; isolated case, parents not tested
-
-
Isolated (sporadic)
00y18m
-
-
-
-
Kristen Nowak
00106223
0000084040
age onset 35y/10y
-
-
Familial, autosomal dominant
-
-
-
-
-
Kristen Nowak
00106225
0000084045
mild, age onset 50y/30y
-
-
Familial, autosomal dominant
-
-
-
-
-
Kristen Nowak
00106230
0000084047
myopathy, nemaline, type 3 (NEM-3);AM;IRM
-
-
Unknown
2m
-
-
-
-
Kristen Nowak
00106232
0000084052
myopathy, nemaline, type 3 (NEM-3); IRM; age onset 64y/34y/33y/3y
-
-
Familial, autosomal dominant
-
-
-
-
-
Kristen Nowak
00106237
0000084054
severe; do not have parental DNA
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106239
0000084055
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106240
0000084056
severe
-
-
Unknown
16y
-
-
-
-
Kristen Nowak
00106241
0000084057
mild
-
-
Unknown
34y
-
-
-
-
Kristen Nowak
00106242
0000084058
mild
-
-
Unknown
44y
-
-
-
-
Kristen Nowak
00106243
0000084059
intermediate
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106244
0000084063
severe
-
-
Isolated (sporadic)
-
-
-
-
-
Alan Beggs
00106248
0000084064
intermediate
-
-
Familial, autosomal recessive
30m
-
-
-
-
Kristen Nowak
00106249
0000084065
severe
-
-
Familial, autosomal recessive
<1y
-
-
-
-
Kristen Nowak
00106250
0000084066
severe
-
-
Familial, autosomal recessive
-
-
-
-
-
Kristen Nowak
00106251
0000084067
severe; parental DNA not available, autosomal recessive, homozygous for the mutation
-
-
Familial, autosomal recessive
<01y
-
-
-
-
Kristen Nowak
00106252
0000084068
intermediate
-
-
Isolated (sporadic)
3y
-
-
-
-
Alan Beggs
00106253
0000084069
severe, age onset 1d/4d
-
-
Familial, autosomal dominant
-
-
-
-
-
Kristen Nowak
00106254
0000084070
severe
-
-
Isolated (sporadic)
13m
-
-
-
-
Kristen Nowak
00106255
0000084071
intermediate
-
-
Isolated (sporadic)
1y
-
-
-
-
Alan Beggs
00106256
0000084072
typical
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106257
0000084073
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106258
0000084075
severe; Tyr190*, small A peak, may be mosaic?
-
-
Familial, autosomal recessive
-
-
-
-
-
Kristen Nowak
00106260
0000084076
intermediate
-
-
Isolated (sporadic)
15m
-
-
-
-
Kristen Nowak
00106261
0000084077
severe
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106262
0000084078
severe
-
-
Unknown
14d
-
-
-
-
Kristen Nowak
00106263
0000084079
-
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106264
0000084080
severe
-
-
Isolated (sporadic)
3m
-
-
-
-
Alan Beggs
00106265
0000084081
-
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106266
0000084082
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106267
0000084083
-
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106268
0000084084
adult onset, mild, progressive; dominant,segregation not confirmed
-
-
Familial, autosomal dominant
-
-
-
-
-
Kristen Nowak
00106269
0000084086
typical
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106271
0000084088
severe
-
-
Unknown
3y
-
-
-
-
Kristen Nowak
00106273
0000084089
severe
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106274
0000084090
typical
-
-
Isolated (sporadic)
3y
-
-
-
-
Alan Beggs
00106275
0000084091
typical
-
-
Isolated (sporadic)
7y
-
-
-
-
Kristen Nowak
00106276
0000084093
severe
-
-
Isolated (sporadic)
14d
-
-
-
-
Kristen Nowak
00106278
0000084094
-
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106279
0000084095
age onset 31y/58y
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106280
0000084096
-
-
-
Isolated (sporadic)
39y
-
-
-
-
Alan Beggs
00106281
0000084097
rods pointed, lower limbs clearly weaker than upper limbs
-
-
Isolated (sporadic)
17y
-
-
-
-
Kristen Nowak
00106282
0000084099
severe; first clinical diagnosis was SMA
-
-
Isolated (sporadic)
7y
-
-
-
-
Kristen Nowak
00106284
0000084100
severe; Disease severity stated in email from Carina to Dr Krcho, copied to Nigel Laing, 17.8.07
-
-
Unknown
-
-
-
-
-
Kristen Nowak
00106285
0000084101
mild
-
-
Unknown
32y
-
-
-
-
Kristen Nowak
00106286
0000084102
mild, childhood onset; founders parents not tested; age onset 8y/14y/16y/39y/40y
-
-
Familial, autosomal dominant
-
-
-
-
-
Alan Beggs
00106287
0000084103
severe
-
-
Isolated (sporadic)
8y
-
-
-
-
Alan Beggs
00106288
0000084104
severe
-
-
Isolated (sporadic)
10y
-
-
-
-
Kristen Nowak
00106289
0000084105
severe
-
-
Unknown
3y9m
-
-
-
-
Kristen Nowak
00106290
0000084106
severe; contractures, no spontaneous movement at birth
-
-
Familial, autosomal recessive
2m
-
-
-
-
Alan Beggs
00106291
0000084107
severe
-
-
Isolated (sporadic)
21m
-
-
-
-
Kristen Nowak
00106292
0000084108
typical; mother does not carry mutation, do not have paternal DNA
-
-
Unknown
5y
-
-
-
-
Kristen Nowak
00106293
0000084109
typical
-
-
Isolated (sporadic)
1y6m
-
-
-
-
Kristen Nowak
00106294
0000084110
-
-
-
Isolated (sporadic)
-
-
-
-
-
Kristen Nowak
00106295
10 per page
25 per page
50 per page
100 per page
Legend
How to query
« First
Prev
1
2
Next
Last »
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our
APIs
to retrieve data.
Powered by
LOVD v.3.0
Build 30b
LOVD software ©2004-2024
Leiden University Medical Center
Database contents © by their respective submitters and curators