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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Example |
Matches |
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Text |
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| | |
Text |
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Text |
!fs |
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| ^ |
Text |
^p.(Arg |
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Text |
="" |
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Text |
="p.0" |
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Text |
!="" |
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Text |
!="p.0" |
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| combination |
Text |
*|Ter !fs |
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|
Date |
2020 |
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| | |
Date |
2020-03|2020-04 |
all entries matching March or April, 2020 |
| ! |
Date |
!2020-03 |
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| < |
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' |
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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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Legend |
How to query |
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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
|
| 0000051426 |
- |
- |
- |
Unknown |
10y |
- |
- |
- |
- |
Johan den Dunnen |
00065310 |
| 0000165773 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217323 |
| 0000165781 |
- |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217331 |
| 0000165782 |
delayed motor development, ptosis, strabismus, scoliosis, amyotrophy |
central core disease |
CCD |
Unknown |
- |
- |
1d |
Hydramnion, fetal akinesia |
- |
Johan den Dunnen |
00217332 |
| 0000165783 |
delayed motor development, ptosis, strabismus |
central core disease |
CCD |
Unknown |
- |
- |
1d |
Arthrogryposis, hypotonia, respiratory mechanical assistance |
- |
Johan den Dunnen |
00217333 |
| 0000165794 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217344 |
| 0000165795 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217345 |
| 0000165796 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217346 |
| 0000165797 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217347 |
| 0000165798 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217348 |
| 0000165799 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217349 |
| 0000165844 |
Cores in muscle biopsy; enhanced CICR test |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217394 |
| 0000165845 |
Cores in muscle biopsy; enhanced CICR test |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217395 |
| 0000165846 |
Proximal muscle weakness; cores in muscle biopsy; enhanced CICR test |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217396 |
| 0000165847 |
Cores in muscle biopsy; enhanced CICR test |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217397 |
| 0000165866 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217416 |
| 0000165892 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217442 |
| 0000165893 |
- |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217443 |
| 0000165894 |
- |
central core disease |
CCD |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217444 |
| 0000165895 |
- |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217445 |
| 0000165896 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217446 |
| 0000165897 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217447 |
| 0000165898 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217448 |
| 0000165899 |
- |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217449 |
| 0000165900 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217450 |
| 0000165903 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217453 |
| 0000165904 |
- |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217454 |
| 0000165940 |
Predominantly axial and proximal weakness; mild scoliosis; CPK elevated (HP:0003236) 153 (19y) |
CCD;MHS1 |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217490 |
| 0000165953 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217503 |
| 0000165955 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217505 |
| 0000165956 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217506 |
| 0000165957 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217507 |
| 0000165958 |
muscle weakness, hip dysplasia, scoliosis |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217508 |
| 0000165959 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217509 |
| 0000165960 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217510 |
| 0000166000 |
- |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217550 |
| 0000166001 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217551 |
| 0000166005 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217555 |
| 0000166007 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217557 |
| 0000166008 |
delayed motor milestones; muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
bilateral congenital hip and hypotonia |
- |
Johan den Dunnen |
00217558 |
| 0000166009 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217559 |
| 0000166010 |
scoliosis; facial weakness |
CCD; MHS1? |
CCD |
Familial, autosomal dominant |
- |
- |
1d |
bilateral congenital dislocation of the hips |
- |
Johan den Dunnen |
00217560 |
| 0000166045 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217595 |
| 0000166054 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217604 |
| 0000166069 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217619 |
| 0000166076 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217626 |
| 0000166077 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217627 |
| 0000166078 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217628 |
| 0000166081 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217631 |
| 0000166095 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217645 |
| 0000166096 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217646 |
| 0000166097 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217647 |
| 0000166110 |
- |
central core disease |
CCD |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217660 |
| 0000166123 |
Cores in muscle biopsy; enhanced CICR test |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217673 |
| 0000166125 |
- |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217675 |
| 0000166134 |
- |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217684 |
| 0000166154 |
Distal muscle weakness; cores in muscle biopsy; abnormally enhanced CICR test |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217704 |
| 0000166178 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217728 |
| 0000166182 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217732 |
| 0000166184 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217734 |
| 0000166185 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217735 |
| 0000166186 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00217736 |
| 0000166187 |
ambulatory, proximal weakness, scoliosis; able to run |
CCD; I-1 |
CCD |
Familial, autosomal dominant |
- |
- |
- |
difficulty running |
- |
Johan den Dunnen |
00217737 |
| 0000166195 |
Cores in muscle biopsy; enhanced CICR test |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217745 |
| 0000166196 |
Abnormally enhanced CICR test |
CCD;MHS1 |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217746 |
| 0000166198 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217748 |
| 0000166199 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
1d |
Poor fetal movements; floppy infant; respiratory insuficiency; poor sucking |
- |
Jorge Oliveira |
00217749 |
| 0000166200 |
Cores in muscle biopsy; delayed motor skills; muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
Floppy infant |
- |
Jorge Oliveira |
00217750 |
| 0000166201 |
Cores in muscle biopsy; delayed motor skills; muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
1d |
Poor fetal movements; floppy infant |
- |
Jorge Oliveira |
00217751 |
| 0000166202 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
Poor fetal movements |
- |
Jorge Oliveira |
00217752 |
| 0000166203 |
Cores in muscle biopsy; muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
Floppy infant |
- |
Jorge Oliveira |
00217753 |
| 0000166204 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217754 |
| 0000166205 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
1d |
Respiratory insuficiency; poor sucking |
- |
Jorge Oliveira |
00217755 |
| 0000166206 |
Cores in muscle biopsy; delayed motor skills; muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
Poor fetal movements |
- |
Jorge Oliveira |
00217756 |
| 0000166207 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217757 |
| 0000166208 |
Cores in muscle biopsy; delayed motor skills; muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
1d |
Poor fetal movements; floppy infant; respiratory insuficiency |
- |
Jorge Oliveira |
00217758 |
| 0000166209 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
Poor fetal movements; floppy infant |
- |
Jorge Oliveira |
00217759 |
| 0000166210 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217760 |
| 0000166211 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
1d |
Poor fetal movements; floppy infant; respiratory insuficiency |
- |
Jorge Oliveira |
00217761 |
| 0000166212 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
Floppy infant |
- |
Jorge Oliveira |
00217762 |
| 0000166213 |
Cores in muscle biopsy; muscle weakness |
central core disease |
CCD |
Unknown |
- |
- |
1d |
Floppy infant; respiratory insuficiency; poor sucking |
- |
Jorge Oliveira |
00217763 |
| 0000166214 |
Cores in muscle biopsy; delayed motor skills; proximal muscle weakness |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
1d |
Floppy infant; respiratory insuficiency; poor sucking |
- |
Jorge Oliveira |
00217764 |
| 0000166238 |
Uniform type 1 fibers in muscle biopsy |
central core disease |
CCD |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217788 |
| 0000166239 |
Muscle pain and fadigue; generalized arthralgia; adverse reaction to succinylcholine ; CPK elevated (HP:0003236) 456 |
central core disease |
CCD |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217789 |
| 0000166240 |
Muscle pain and fadigue; myopathic EMG; CPK not elevated (-HP:0003236) |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217790 |
| 0000166241 |
Muscle pain and fadigue; cardio-respiratory arrest and radbomyolisis during anaesthestic procedure ; CPK elevated (HP:0003236) 619 |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217791 |
| 0000166245 |
- |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217795 |
| 0000166246 |
CPK not elevated (-HP:0003236); able to run |
central core disease |
CCD |
Familial |
- |
9y |
- |
- |
- |
Jorge Oliveira |
00217796 |
| 0000166247 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217797 |
| 0000166248 |
- |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217798 |
| 0000166249 |
- |
central core disease |
CCD |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217799 |
| 0000166250 |
facial weakness; muscle hypotrophy; CPK not elevated (-HP:0003236) |
central core disease |
CCD |
Familial, autosomal recessive |
- |
42y |
- |
- |
- |
Jorge Oliveira |
00217800 |
| 0000166251 |
surgically corrected foot deformities |
central core disease |
CCD |
Familial, autosomal recessive |
- |
46y |
- |
- |
- |
Jorge Oliveira |
00217801 |
| 0000166322 |
CPK not elevated (-HP:0003236) |
central core disease |
CCD |
Familial |
- |
- |
10y |
difficulty climbing stairs and rising from siting position |
- |
Jorge Oliveira |
00217872 |
| 0000166328 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217878 |
| 0000166329 |
- |
central core disease |
CCD |
Unknown |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217879 |
| 0000166330 |
Predominant proximal weakness; extra-ocular muscle involvement; CPK elevated (HP:0003236) 89; walk 18m;not sitting 14y |
CCD;CNM-ad |
CCD |
Isolated (sporadic) |
- |
- |
- |
Hypotony, reduced antigravity movements, feeding problems |
- |
Jorge Oliveira |
00217880 |
| 0000166332 |
Generalized weakness; feeding difficulties; respiratory impairment; malignant hyperthermia |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217882 |
| 0000166333 |
Predominant distal weakness |
central core disease |
CCD |
Familial |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217883 |
| 0000166334 |
Predominant proximal weakness |
central core disease |
CCD |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Jorge Oliveira |
00217884 |
|
|
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