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Phenotypes for disease #04168 (CNM (myopathy, centronuclear (CNM)))
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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Date
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Date
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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 on or after June 15th, 2020
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Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
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all entries exactly matching 23
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all entries exactly matching 23 or 24
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Numeric
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all entries not exactly matching 23
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Numeric
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all entries lower than 23
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all entries lower than, or equal to, 23
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Numeric
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all entries with values from 20 to 29, but not equal to 23
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all entries containing 'South Asian', but not containing 'South East Asian'
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517 entries on 6 pages. Showing entries 1 - 100.
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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000023255
see paper; early death (2d, 2d, 3w)
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00027184
0000023256
severe hypotonia since birth; needed tracheostomy; 24 hr mechanical ventilation; gastrostomy; dilated cardiomyopathy; congestive cardiac failure in neonatal age was treated with digoxin and captopril; hypotrophic myofibers, marked increase in central nuclei
-
-
Isolated (sporadic)
06y
-
-
-
-
Johan den Dunnen
00027185
0000023257
hypotonia since birth, dilated cardiomyopathy and nephrolithiasis, orogastric feeds, no assisted ventilation; myopathic changes; variation in fiber size, more prominent in some fascicles, increased central nuclei in hypotrophic fibers, predominant type 1 fibers
-
-
Familial, autosomal recessive
01y06m
-
-
-
-
Johan den Dunnen
00027186
0000045035
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Claire Chauveau
00058404
0000045036
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Claire Chauveau
00058405
0000045037
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Claire Chauveau
00058406
0000045038
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Claire Chauveau
00058407
0000045039
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Claire Chauveau
00058408
0000050426
0.20 central nuclei, minicores, type I predominance/no hypertrophy; respiratory problems (HP:0002093) at birth not at last exam, feeding problems (HP:0011968) at birth, hypotonia (HP:0001252) at birth, delayed motor milestones (HP:0001270), no abnormality extraocular muscles (-HP:0008049), scoliosis (HP:0002650), contractures ankles (HP:0006466)
-
-
Familial, autosomal recessive
10y
-
00y00m00d
-
-
Johan den Dunnen
00063838
0000070548
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092216
0000070549
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092218
0000070550
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092219
0000070551
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092220
0000070552
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092221
0000070553
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092222
0000070554
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092223
0000070555
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092224
0000070556
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092225
0000070557
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092226
0000070558
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092227
0000070559
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092228
0000070560
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092229
0000070561
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092230
0000070562
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092231
0000070563
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092232
0000070565
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092233
0000070566
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092234
0000070567
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092236
0000070568
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Osorio Abath Neto
00092237
0000073339
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00092235
0000117239
pronounced myalgia, exercise intolerance, large muscle mass, childhood onset in youngest generation, mild cognitive features
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00144502
0000159964
Severe, additional hypospadias
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Johan den Dunnen
00211483
0000159965
Severe
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Johan den Dunnen
00211484
0000159966
Severe
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211485
0000159967
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211486
0000159968
Mild
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211487
0000159969
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211488
0000159970
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211489
0000159971
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211490
0000159972
Severe
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211491
0000159973
Severe
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211492
0000159974
?
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211493
0000159975
Moderate; walk-17m
myotubular myopathy
CNMX
Unknown
-
-
-
decreased fetal movements, feeding difficulties
-
Jorge Oliveira
00211494
0000159976
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211495
0000159977
?
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211496
0000159978
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211497
0000159979
?
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211498
0000159980
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211499
0000159981
?
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211500
0000159982
Mild; walk
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211501
0000159983
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211502
0000159984
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211503
0000159985
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
<1m
neonatal hypotony, required respiratory support
-
Jorge Oliveira
00211504
0000159986
?
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211505
0000159987
severe, neonatal death
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211506
0000159988
severe, neonatal death
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211507
0000159989
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211508
0000159990
-
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211509
0000159991
-
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211510
0000159992
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211511
0000159993
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211512
0000159994
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211513
0000159995
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211514
0000159996
-
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
<0d
Polyhydramnios and reduced fetal movement
-
Jorge Oliveira
00211515
0000159997
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211516
0000159998
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211517
0000159999
severe, neonatal death
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211518
0000160000
severe, neonatal death
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211519
0000160001
severe, neonatal death
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211520
0000160002
Mild
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211521
0000160003
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211522
0000160004
severe, neonatal death
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211523
0000160005
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211524
0000160006
-
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211525
0000160007
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211526
0000160008
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211527
0000160009
Mild or moderate
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211528
0000160010
Mild
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211529
0000160011
-
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211530
0000160012
Mild
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211531
0000160013
?
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211532
0000160014
Mild or moderate
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211533
0000160015
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211534
0000160016
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211535
0000160017
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211536
0000160018
?
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211537
0000160019
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211538
0000160020
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211539
0000160021
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211540
0000160022
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211541
0000160023
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211542
0000160024
?
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211543
0000160025
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211544
0000160026
Severe
myotubular myopathy
CNMX
Unknown
-
-
-
-
-
Jorge Oliveira
00211545
0000160027
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211546
0000160028
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211547
0000160029
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211548
0000160030
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211549
0000160031
Severe
myotubular myopathy
CNMX
Familial
-
-
-
-
-
Jorge Oliveira
00211550
0000160032
Severe
myotubular myopathy
CNMX
Isolated (sporadic)
-
-
-
-
-
Jorge Oliveira
00211551
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