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 #05358 (BTHLM (myopathy, Bethlem (BTHLM)))
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.
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
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.
38 entries on 1 page. Showing entries 1 - 38.
10 per page
25 per page
50 per page
100 per page
Legend
How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000119161
-
-
childhood onset slowly progressive limb-girdle myopathy with joint contractures in fingers ("prayer sign")
Familial, autosomal dominant
-
46y
-
Bethlem myopathy
-
Payam Soltanzadeh
00146420
0000285995
-
-
Global developmental delay, Delayed ability to walk, Motor delay, Delayed gross motor development
Unknown
-
-
-
-
-
Andreas Laner
00392748
0000305556
congenital myopathy
-
see paper; ..., myopathy; unremarkable pregnancy; 1d-hypotonia, soft skin, delayed motor milestones
Familial, autosomal recessive
41y
-
-
-
-
Johan den Dunnen
00411326
0000331960
Bethlem myopathy
BTHLM1
CK <170 IU/L; MRI muscle typical; muscle biopsy lobulated fibers; onset childhood; weakness facial, cervical, proximal UL and LL; contractures wrists, interphalangeal, ankles; scoliosis; no cutaneous alterations; non invasive mechanical ventilation
Unknown
-
43y
-
floppy newborn
-
Johan den Dunnen
00442613
0000331961
Bethlem myopathy
BTHLM1
CK 450 IU/L; MRI muscle typical; muscle biopsy dystrophy; weakness proximal UL and LL; contractures interphalangeal, ankles; no scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
49y
-
weakness
-
Johan den Dunnen
00442614
0000331962
Bethlem myopathy
-
CK <170 IU/L; MRI muscle typical; muscle biopsy dystrophy; onset childhood; weakness cervical, proximal UL and LL; contractures elbows, wrists, interphalangeal, ankles; no scoliosis; cigarette paper scars; non invasive mechanical ventilation
Unknown
-
72y
-
clumsiness, contractures
-
Johan den Dunnen
00442615
0000331963
Bethlem myopathy
-
CK 2800 IU/L; MRI muscle unilateral medial gastrocnemius peripheral infiltration; muscle biopsy minimum non-specific changes; no weaknes; contractures interphalangeal, ankles; no scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
31y
-
hyperckemia
-
Johan den Dunnen
00442616
0000331964
Bethlem myopathy
-
CK 570 IU/L; MRI muscle normal; no weaknes; contractures interphalangeal, ankles; no scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
33y
-
asymptomatic
-
Johan den Dunnen
00442617
0000331965
Bethlem myopathy
-
CK <170 IU/L; MRI muscle normal; weakness cervical, fingers, proximal LL; contractures interphalangeal, ankles; scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
61y
-
asymptomatic
-
Johan den Dunnen
00442618
0000331966
Bethlem myopathy
BTHLM1
CK 1200 IU/L; MRI muscle typical; muscle biopsy dystrophy; weakness proximal UL and LL; contractures interphalangeal, knees; no scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
42y
35y
weakness
-
Johan den Dunnen
00442619
0000331967
Bethlem myopathy
-
CK <170 IU/L; MRI muscle typical; onset childhood; weakness proximal and distal UL, proximal LL; contractures elbows, wrists, interphalangeal; no scoliosis; hyper-keratosis; no entilatory insufficiency
Unknown
-
65y
-
weakness, contractures
-
Johan den Dunnen
00442620
0000331968
Bethlem myopathy
BTHLM1
CK 230 IU/L; MRI muscle typical; muscle biopsy dystrophy; weakness facial, cervical, proximal UL and LL; contractures interphalangeal; no scoliosis; cheloids; no entilatory insufficiency
Unknown
-
59y
50y
weakness
-
Johan den Dunnen
00442621
0000331969
Bethlem myopathy
BTHLM1
CK 800 IU/L; MRI muscle typical; muscle biopsy dystrophy; onset childhood; weakness cervical, proximal UL and LL; contractures elbows, ankles; no scoliosis; no cutaneous alterations; reduced maximal expiratory pressure
Unknown
-
27y
-
weakness
-
Johan den Dunnen
00442622
0000331970
Bethlem myopathy
-
CK 4000 IU/L; MRI muscle typical; muscle biopsy dystrophy, rimmed vacuoles; onset childhood; weakness proximal LL; contractures interphalangeal, ankles; no scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
42y
-
weakness
-
Johan den Dunnen
00442623
0000331971
Bethlem myopathy
-
CK 1000 IU/L; MRI muscle typical; no weaknes; contractures interphalangeal, ankles; no scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
48y
-
hyperckemia
-
Johan den Dunnen
00442624
0000331972
Bethlem myopathy
-
CK 250 IU/L; MRI muscle typical; muscle biopsy dystrophy; weakness distal UL and proximal LL; no contractures; no scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
63y
40y
weakness
-
Johan den Dunnen
00442625
0000331973
Bethlem myopathy
-
CK <170 IU/L; MRI muscle typical; muscle biopsy dystrophy; weakness distal UL and proximal LL; no contractures; no scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
67y
64y
weakness
-
Johan den Dunnen
00442626
0000331974
Bethlem myopathy
-
CK 220 IU/L; MRI muscle typical; weakness proximal UL and LL; contractures interphalangeal, wrists; no scoliosis; cheloids; no entilatory insufficiency
Unknown
-
55y
52y
weakness
-
Johan den Dunnen
00442627
0000331975
Bethlem myopathy
BTHLM1
CK 830 IU/L; MRI muscle typical; onset childhood; weakness distal LL; contractures interphalangeal, ankles; no scoliosis; no cutaneous alterations; no entilatory insufficiency
Unknown
-
19y
-
weakness, contractures
-
Johan den Dunnen
00442628
0000334235
Bethlem myopathy
BTHLM1
-
Familial, autosomal recessive
-
-
-
-
-
Victor Morel
00444985
0000334236
Bethlem myopathy
BTHLM1
-
Familial, autosomal recessive
-
-
03y
-
-
Victor Morel
00444986
0000334237
Bethlem myopathy
BTHLM1
-
Familial, autosomal recessive
-
-
04y
-
-
Victor Morel
00444986
0000334263
Bethlem myopathy
BTHLM1
congenital feet deformity walking difficulties at 47yo
Familial, autosomal recessive
49y
49y
47y
-
-
Victor Morel
00445011
0000334264
Bethlem myopathy
BTHLM1
-
Unknown
-
-
-
-
-
Victor Morel
00445012
0000334265
Bethlem myopathy
BTHLM1
-
Familial, autosomal recessive
-
-
00y18m
-
-
Victor Morel
00445013
0000334266
Bethlem myopathy
BTHLM1
difficulties to run during childhood; 55y-difficulties to walk
Unknown
-
55y
08y
-
-
Victor Morel
00445014
0000334268
Bethlem myopathy
BTHLM1
-
Familial, autosomal dominant
-
15y
04y
-
-
Victor Morel
00445016
0000334269
Bethlem myopathy
BTHLM1
-
Unknown
-
07y
02y
-
-
Victor Morel
00445017
0000334270
Bethlem myopathy
UCDM1
-
Familial, autosomal dominant
02y
-
02y
-
-
Victor Morel
00445017
0000334271
Bethlem myopathy
BTHLM1
-
Familial, autosomal dominant
-
-
51y
-
-
Victor Morel
00445018
0000334273
Bethlem myopathy
UCDM1
Loss of walk at 10yo
Unknown
-
03y
03y
-
-
Victor Morel
00445020
0000334274
Bethlem myopathy
BTHLM1
-
Unknown
-
12y
00y
-
-
Victor Morel
00445021
0000334275
Bethlem myopathy
UCDM1
-
Unknown
-
00y18m
00y03m
-
-
Victor Morel
00445022
0000334277
Bethlem myopathy
BTHLM1
-
Di-genic
-
43y
08y
-
-
Victor Morel
00445024
0000334393
Bethlem myopathy
BTHLM1
see paper; ...
Familial, autosomal recessive
-
-
-
-
-
Victor Morel
00445139
0000334394
Bethlem myopathy
BTHLM1
see paper; ...
Familial, autosomal recessive
-
-
-
-
-
Victor Morel
00445140
0000334396
Bethlem myopathy
BTHLM1
see paper; ...
Familial, autosomal recessive
-
-
-
-
-
Victor Morel
00445142
0000334397
Bethlem myopathy
BTHLM1
see paper; ...
Familial, autosomal recessive
-
-
-
-
-
Victor Morel
00445143
10 per page
25 per page
50 per page
100 per page
Legend
How to query
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