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

 Phenotype ID
|

 Phenotype details
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Protein
|

 Owner
|

 Individual ID
|
| 0000231244 |
Increasing muscle weakness, cramps |
- |
- |
Unknown |
43y |
- |
- |
- |
- |
Andreas Laner |
00305394 |
| 0000231246 |
Muscle stiffness, muscle pain in the legs, left hip flexor paresis |
- |
- |
Unknown |
- |
- |
- |
38y |
- |
Andreas Laner |
00305396 |
| 0000321329 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430545 |
| 0000321330 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430546 |
| 0000321331 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430547 |
| 0000321332 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430548 |
| 0000321333 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430549 |
| 0000321334 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430550 |
| 0000321335 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430551 |
| 0000321336 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430552 |
| 0000321337 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430553 |
| 0000321338 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430554 |
| 0000321339 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430555 |
| 0000321340 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430556 |
| 0000321341 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430557 |
| 0000321342 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430558 |
| 0000321343 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430559 |
| 0000321344 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430560 |
| 0000321345 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430561 |
| 0000321346 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430562 |
| 0000321347 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430563 |
| 0000321348 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430564 |
| 0000321349 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430565 |
| 0000321350 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430566 |
| 0000321351 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430567 |
| 0000321352 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430568 |
| 0000321353 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430569 |
| 0000321354 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430570 |
| 0000321355 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430571 |
| 0000321356 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430572 |
| 0000321357 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430573 |
| 0000321358 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430574 |
| 0000321359 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430575 |
| 0000321360 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430576 |
| 0000321361 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430577 |
| 0000321362 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430578 |
| 0000321363 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430579 |
| 0000321364 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430580 |
| 0000321365 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430581 |
| 0000321366 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430582 |
| 0000321367 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430583 |
| 0000321368 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430584 |
| 0000321369 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430585 |
| 0000321370 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430586 |
| 0000321371 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430587 |
| 0000321372 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430588 |
| 0000321373 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430589 |
| 0000321374 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430590 |
| 0000321375 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430591 |
| 0000321376 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430592 |
| 0000321377 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430593 |
| 0000321378 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430594 |
| 0000321379 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430595 |
| 0000321380 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430596 |
| 0000321381 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430597 |
| 0000321382 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430598 |
| 0000321383 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430599 |
| 0000321384 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430600 |
| 0000321385 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430601 |
| 0000321386 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430602 |
| 0000321387 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430603 |
| 0000321388 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430604 |
| 0000321389 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430605 |
| 0000321390 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430606 |
| 0000321391 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430607 |
| 0000321392 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430608 |
| 0000321393 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430609 |
| 0000321394 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430610 |
| 0000321395 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430611 |
| 0000321396 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430612 |
| 0000321397 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430613 |
| 0000321398 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430614 |
| 0000321399 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430615 |
| 0000321400 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430616 |
| 0000321401 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430617 |
| 0000321402 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430618 |
| 0000321403 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430619 |
| 0000321404 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430620 |
| 0000321405 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430621 |
| 0000321406 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430622 |
| 0000321407 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430623 |
| 0000321408 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430624 |
| 0000321409 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430625 |
| 0000321410 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430626 |
| 0000321411 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430627 |
| 0000321412 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430628 |
| 0000321413 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430629 |
| 0000321414 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430630 |
| 0000321415 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430631 |
| 0000321416 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430632 |
| 0000321417 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430633 |
| 0000321418 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430634 |
| 0000321419 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430635 |
| 0000321420 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430636 |
| 0000321421 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430637 |
| 0000321422 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430638 |
| 0000321423 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430639 |
| 0000321424 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430640 |
| 0000321425 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430641 |
| 0000321426 |
- |
myotonic dystrophy |
DM2 |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00430642 |