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

 Phenotype ID
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Phenotype details
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Owner
|

 Individual ID
|
0000187328 |
- |
- |
see paper; ... |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00248331 |
0000187329 |
neuromuscular disorder |
- |
see paper; … |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00248332 |
0000187330 |
neuromuscular disorder |
- |
see paper; … |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00248333 |
0000187331 |
neuromuscular disorder |
- |
see paper; … |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00248334 |
0000187332 |
neuromuscular disorder |
- |
see paper; … |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00248335 |
0000187333 |
neuromuscular disorder |
- |
see paper; … |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00248336 |
0000187334 |
neuromuscular disorder |
- |
see paper; … |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00248337 |
0000187335 |
neuromuscular disorder |
- |
see paper; … |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00248338 |
0000187336 |
neuromuscular disorder |
- |
see paper; … |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00248339 |
0000289186 |
CMT |
RS1 |
see paper; ... |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00396023 |
0000289187 |
LGMD |
RS1 |
see paper; ... |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00396024 |
0000289188 |
CMT |
RS1 |
see paper; ... |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00396025 |
0000289189 |
LGMD |
RS1 |
see paper; ... |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00396026 |
0000289190 |
LGMD |
RS1 |
see paper; ... |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00396027 |
0000289191 |
LGMD |
RS1 |
see paper; ... |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00396028 |
0000289192 |
LGMD |
RS1 |
see paper; ... |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00396029 |
0000289193 |
CMT |
RS1 |
see paper; ... |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00396030 |
0000289194 |
LGMD |
- |
see paper; ... |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00396031 |
0000292072 |
congenital myopathy |
- |
serum CK <200 U/L; muscle biopsy central cores; polyhydramnios, severe neonatal hypotonia, limb-girdle weakness, facial hypomimia |
Unknown |
- |
- |
<0d |
- |
Johan den Dunnen |
00398984 |
0000292073 |
limb-girdle muscular dytrophy |
- |
limb-girdle muscle weakness |
Unknown |
- |
- |
>18y |
- |
Johan den Dunnen |
00398985 |
0000292074 |
neuromuscular disorder |
- |
serum CK 1844 U/L; quadriceps hypertrophy |
Unknown |
- |
- |
16y |
- |
Johan den Dunnen |
00398986 |
0000292075 |
congenital myasthenic syndrome |
- |
serum CK <200 U/L; weakness and myasthenic crises |
Unknown |
- |
- |
2y |
- |
Johan den Dunnen |
00398987 |
0000292076 |
COL6-realted myopathy |
- |
distal contractures, skin biopsy compatible with bethlem myopathy |
Unknown |
- |
- |
2y |
- |
Johan den Dunnen |
00398988 |
0000292077 |
neuromuscular disorder |
- |
serum CK normal; muscle biopsy yype 1 fiber predominance; plagiocephaly, microcephaly, hypotonia |
Unknown |
- |
- |
8m |
- |
Johan den Dunnen |
00398989 |
0000292078 |
neuromuscular disorder |
- |
serum CK normal |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00398990 |
0000292079 |
neuromuscular disorder |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00398991 |
0000292080 |
neuromuscular disorder |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00398992 |
0000292081 |
limb-girdle muscular dytrophy |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00398993 |
0000292082 |
neuromuscular disorder |
- |
muscle biopsy dystrophic pattern; axial and peripheral hypotonia |
Unknown |
- |
- |
1d |
- |
Johan den Dunnen |
00398994 |
0000292083 |
myofibrillar myopathy |
- |
serum CK 374 U/L; muscle biopsy myofibrillar myopathy; leg and joint pain |
Unknown |
- |
- |
54y |
- |
Johan den Dunnen |
00398995 |
0000292084 |
neuromuscular disorder |
- |
serum CK 958 U/L; muscle biopsy yype 1 fiber predominance, atrophic fibers; paresis scapular waist with left predominanc |
Unknown |
- |
- |
43y |
- |
Johan den Dunnen |
00398996 |
0000292085 |
neuromuscular disorder |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00398997 |
0000292086 |
neuromuscular disorder |
- |
serum CK 559 U/L; muscle biopsy fiber size variability, central nuclei and inflammatory ; posterior distal weakness, cardiomyopathy |
Unknown |
- |
- |
68y |
- |
Johan den Dunnen |
00398998 |
0000292087 |
dysferlinopathy |
- |
serum CK 3661 U/L; muscle biopsy dystrophic pattern, IHC no DYSF; limb-girdle muscle weakness |
Unknown |
- |
- |
24y |
- |
Johan den Dunnen |
00398999 |
0000292088 |
neuromuscular disorder |
- |
serum CK 295 U/L; muscle biopsy myopathic changes, rimmed vacuoles; axial muscle atrophy, severe weakness lower limbs |
Unknown |
- |
- |
24y |
- |
Johan den Dunnen |
00399000 |
0000292089 |
limb-girdle muscular dytrophy |
- |
raised serum CK 6-10 fold; muscle biopsy dystrophic pattern |
Unknown |
- |
- |
10y-20y |
- |
Johan den Dunnen |
00399001 |
0000292090 |
limb-girdle muscular dytrophy |
- |
serum CK 2217 U/L; muscle biopsy dystrophic pattern |
Unknown |
- |
- |
18y |
- |
Johan den Dunnen |
00399002 |
0000292091 |
congenital myopathy |
- |
muscle biopsy central cores |
Unknown |
- |
- |
1d |
- |
Johan den Dunnen |
00399003 |
0000292092 |
centronuclear myopathy |
- |
muscle biopsy internal nuclei 0.80 fibers; proximal muscle weakness in upper and lower limbs |
Unknown |
- |
- |
49y |
- |
Johan den Dunnen |
00399004 |
0000292093 |
neuromuscular disorder |
- |
serum CK >1300 U/L; muscle biopsy small protein aggregates; distal muscle weakness |
Unknown |
- |
- |
53y |
- |
Johan den Dunnen |
00399005 |
0000292094 |
neuromuscular disorder |
- |
serum CK 159 U/L; muscle biopsy unspecific myopathic changes; asymmetric distal weakness lower limbs, myalgias, anterior tibial weakness |
Unknown |
- |
- |
74y |
- |
Johan den Dunnen |
00399006 |
0000292095 |
neuromuscular disorder |
- |
serum CK 112 U/L; limb-girdle muscle weakness |
Unknown |
- |
- |
9y |
- |
Johan den Dunnen |
00399007 |
0000292096 |
congenital myopathy |
- |
serum CK 122 U/L; hypotonia, axial muscle weakness weakness |
Unknown |
- |
- |
20m |
- |
Johan den Dunnen |
00399008 |
0000292097 |
congenital myopathy |
- |
serum CK <200 U/L; muscle biopsy central cores; hypotonia |
Familial, X-linked recessive |
- |
- |
<00y01m |
- |
Johan den Dunnen |
00399009 |
0000292098 |
COL6-realted myopathy |
- |
serum CK 270 U/L; muscle biopsy dystrophic changes, COLVI reduction in muscle and skin biopsy ; hypotonia, congenital torticollis, limb- girdle weakness, multiple retractions |
Unknown |
- |
- |
<1m |
- |
Johan den Dunnen |
00399010 |
0000292099 |
neuromuscular disorder |
- |
muscle biopsy vacuoles; limb-girdle muscle weakness |
Unknown |
- |
- |
14y |
- |
Johan den Dunnen |
00399011 |
0000292100 |
congenital myopathy |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399012 |
0000292101 |
COL6-realted myopathy |
- |
serum CK 749 U/L; reduced collagen vi expression in skin biopsy |
Unknown |
- |
- |
4y |
- |
Johan den Dunnen |
00399013 |
0000292102 |
limb-girdle muscular dytrophy |
- |
serum CK 1862 U/L; muscle biopsy dystrophic pattern, macrophage infiltration ; limb-girdle muscle weakness |
Unknown |
- |
- |
14y |
- |
Johan den Dunnen |
00399014 |
0000292103 |
neuromuscular disorder |
- |
muscle biopsy dystrophic pattern, rimmed vacuoles, protein aggregates |
Unknown |
- |
- |
30y |
- |
Johan den Dunnen |
00399015 |
0000292104 |
neuromuscular disorder |
- |
limb-girdle muscle weakness, limb contractures |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399016 |
0000292105 |
neuromuscular disorder |
- |
distal muscle weakness, pes cavus |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399017 |
0000292106 |
centronuclear myopathy |
- |
serum CK 103 U/L; muscle biopsy myopathic changes with central nuclei |
Unknown |
- |
- |
<1m |
- |
Johan den Dunnen |
00399018 |
0000292107 |
congenital myopathy |
- |
serum CK normal; muscle biopsy multiminicores |
Unknown |
- |
- |
1d |
- |
Johan den Dunnen |
00399019 |
0000292108 |
congenital myasthenic syndrome |
- |
hypotonia, diplegic facies, palpebral ptosis, limb-girdle weakness |
Unknown |
- |
- |
1d |
- |
Johan den Dunnen |
00399020 |
0000292109 |
neuromuscular disorder |
- |
muscle biopsy congenital fiber type disproportion |
Unknown |
- |
- |
1d |
- |
Johan den Dunnen |
00399021 |
0000292110 |
neuromuscular disorder |
- |
raised serum CK 2 fold; muscle biopsy isolated fibers with rimmed vacuoles |
Unknown |
- |
- |
20y |
- |
Johan den Dunnen |
00399022 |
0000292111 |
neuromuscular disorder |
- |
serum CK 1148 U/L; muscle biopsy rimmed vacuoles; hereditary inclusion body myositis |
Unknown |
- |
- |
44y |
- |
Johan den Dunnen |
00399023 |
0000292112 |
LAMA2-related congenital muscular dystrophy |
- |
serum CK 2286 U/L; muscle biopsy dystrophic pattern, partial merosin deficiency |
Unknown |
- |
- |
18m |
- |
Johan den Dunnen |
00399024 |
0000292113 |
neuromuscular disorder |
- |
serum CK 91 U/L; muscle biopsy internal nuclei; cardiomyopathy, axial weakness |
Unknown |
- |
- |
50y |
- |
Johan den Dunnen |
00399025 |
0000292114 |
neuromuscular disorder |
- |
raised serum CK 20 fold; muscle biopsy dystrophic pattern; distal and asymmetric limb-girdle muscle dystrophy |
Unknown |
- |
- |
27y |
- |
Johan den Dunnen |
00399026 |
0000292115 |
neuromuscular disorder |
- |
serum CK 456 U/L; muscle biopsy myopathic changes; distal muscle atrophy, fat degeneration of tibialis anterior |
Unknown |
- |
- |
41y |
- |
Johan den Dunnen |
00399027 |
0000292116 |
neuromuscular disorder |
- |
raised serum CK 3 fold; muscle biopsy myopathic changes; asymmetric calf atrophy |
Unknown |
- |
- |
30y-40y |
- |
Johan den Dunnen |
00399028 |
0000292117 |
congenital myopathy |
- |
serum CK normal; muscle biopsy internal nuclei |
Unknown |
- |
- |
00y-10y |
- |
Johan den Dunnen |
00399029 |
0000292118 |
congenital myopathy |
- |
serum CK normal; muscle biopsy myopathic changes, predominance type 1 fibers |
Unknown |
- |
- |
1d |
- |
Johan den Dunnen |
00399030 |
0000292119 |
neuromuscular disorder |
- |
serum CK 173 U/L |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399031 |
0000292120 |
neuromuscular disorder |
- |
serum CK 781 U/L |
Unknown |
- |
- |
10y |
- |
Johan den Dunnen |
00399032 |
0000292121 |
COL6-realted myopathy |
- |
dry skin with hyperkeratosis, joint hyperlaxity, bilateral and symmetric atrophy, atrophy with fatty infiltration muscle groups both shoulder girdles |
Unknown |
- |
- |
1d |
- |
Johan den Dunnen |
00399033 |
0000292122 |
neuromuscular disorder |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399034 |
0000292123 |
neuromuscular disorder |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399035 |
0000292124 |
neuromuscular disorder |
- |
serum CK normal; muscle biopsy myopathic changes; hypomimia, severe scoliosis, respiratory insufficiency, axial hypotonia |
Unknown |
- |
- |
1d |
- |
Johan den Dunnen |
00399036 |
0000292125 |
neuromuscular disorder |
- |
serum CK normal; muscle biopsy congenital fiber type disproportion; scoliosis, myopathic facies, generalized hypotonia |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399037 |
0000292126 |
congenital myopathy |
- |
muscle biopsy central cores |
Unknown |
66y |
- |
1d |
- |
Johan den Dunnen |
00399038 |
0000292127 |
distal myopathy |
- |
serum CK 502 U/L; muscle biopsy myopathic changes; distal atrophy lower limb |
Unknown |
36y |
- |
57y |
- |
Johan den Dunnen |
00399039 |
0000292128 |
congenital myopathy |
- |
serum CK <200 U/L; muscle biopsy congenital fiber type disproportion; hypotonia |
Unknown |
17y |
- |
<1m |
- |
Johan den Dunnen |
00399040 |
0000292129 |
neuromuscular disorder |
BMD |
muscle biopsy reduced dystrophin |
Familial, X-linked recessive |
00y |
- |
- |
- |
Johan den Dunnen |
00399041 |
0000292130 |
congenital myopathy |
- |
serum CK normal; muscle biopsy internal nuclei |
Unknown |
0y |
- |
38y |
- |
Johan den Dunnen |
00399042 |
0000292131 |
neuromuscular disorder |
- |
serum CK normal; muscle biopsy rimmed vacuoles, protein aggregates ; muscle weakness |
Unknown |
- |
- |
70y |
- |
Johan den Dunnen |
00399043 |
0000292132 |
neuromuscular disorder |
- |
serum CK normal; muscle biopsy neurogenic pattern |
Unknown |
- |
- |
00y-10y |
- |
Johan den Dunnen |
00399044 |
0000292133 |
COL6-realted myopathy |
- |
raised serum CK 2 fold; muscle biopsy yype 1 fiber predominance |
Unknown |
- |
- |
20y-30y |
- |
Johan den Dunnen |
00399045 |
0000292134 |
neuromuscular disorder |
- |
serum CK 994 U/L; muscle biopsy myopathic changes, rimmed vacuoles; selective atrophy of right radial carpal extensors and left tibialis anterior |
Unknown |
- |
- |
38y |
- |
Johan den Dunnen |
00399046 |
0000292135 |
myofibrillar myopathy |
- |
muscle biopsy predominance type 1 fibers, ring fibers |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399047 |
0000292136 |
nemaline myopathy |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399048 |
0000292137 |
neuromuscular disorder |
- |
serum CK 87 U/L; muscle biopsy central cores; exercise intolerance |
Unknown |
- |
- |
<2y |
- |
Johan den Dunnen |
00399049 |
0000292138 |
centronuclear myopathy |
- |
serum CK normal; muscle biopsy internal nuclei |
Unknown |
- |
- |
60y |
- |
Johan den Dunnen |
00399050 |
0000292139 |
neuromuscular disorder |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399051 |
0000292140 |
neuromuscular disorder |
- |
raised serum CK 3 fold; muscle biopsy normal; limb-girdle muscle weakness, hyperCKemia |
Unknown |
- |
- |
30y-40y |
- |
Johan den Dunnen |
00399052 |
0000292141 |
congenital myasthenic syndrome |
- |
fatigability |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399053 |
0000292142 |
congenital myasthenic syndrome |
- |
serum CK normal; muscle biopsy normal; generalized muscle weakness, reported consanguinity |
Unknown |
- |
- |
1d |
- |
Johan den Dunnen |
00399054 |
0000292143 |
neuromuscular disorder |
- |
muscle biopsy cores and cytoplasmic bodies; hyperckemia, ptosis, arched palate |
Unknown |
- |
- |
31y |
- |
Johan den Dunnen |
00399055 |
0000292144 |
congenital myopathy/congenital myasthenic syndrome |
- |
serum CK <200 U/L; muscle biopsy congenital fiber type disproportion; hypotonia |
Unknown |
- |
- |
<1m |
- |
Johan den Dunnen |
00399056 |
0000292145 |
neuromuscular disorder |
- |
raised serum CK 3 fold; muscle biopsy myopathic changes |
Unknown |
- |
- |
40y-50y |
- |
Johan den Dunnen |
00399057 |
0000292146 |
congenital myasthenic syndrome |
- |
serum CK <200 U/L; muscle biopsy fiber size variability; fatigability |
Unknown |
- |
- |
18m |
- |
Johan den Dunnen |
00399058 |
0000292147 |
centronuclear myopathy |
- |
serum CK 78 U/L; muscle biopsy myopathic changes; hypotonia, muscle weakness |
Unknown |
- |
- |
1y |
- |
Johan den Dunnen |
00399059 |
0000292148 |
neuromuscular disorder |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399060 |
0000292149 |
limb-girdle muscular dytrophy |
- |
muscle biopsy dystrophic pattern; limb-girdle muscle weakness |
Unknown |
- |
- |
25y |
- |
Johan den Dunnen |
00399061 |
0000292150 |
TTN-related limb-girdle muscular dytrophy |
- |
serum CK 145 U/L; muscle biopsy normal; significant pelvic and scapular weakness |
Unknown |
- |
- |
50y |
- |
Johan den Dunnen |
00399062 |
0000292151 |
neuromuscular disorder |
- |
- |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00399063 |
0000292152 |
COL6-realted myopathy |
- |
serum CK 350 U/L; hypotonia, COLVI reduction skin biopsy |
Unknown |
- |
- |
<1m |
- |
Johan den Dunnen |
00399064 |
0000292153 |
congenital myopathy |
- |
serum CK 76 U/L; muscle biopsy central cores; hypotonia |
Unknown |
- |
- |
<1m |
- |
Johan den Dunnen |
00399065 |