Global Variome shared LOVD
DMD (dystrophin)
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Curator:
Johan den Dunnen
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Phenotypes for disease #04312 (CMS (myasthenic syndrome, congenital (CMS)))
Legend
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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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677 entries on 7 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
0000044533
42y-mild bilateral lid ptosis, mild facial weakness, normal function axial muscles, glutei/psoas muscles slightly weak (MRC4+/5), difficulty walking on heels, thorax/pelvis thin
-
-
Isolated (sporadic)
-
-
-
unable to run since early childhood, right-lid ptosis
-
Johan den Dunnen
00057882
0000044534
difficulties running since early childhood, fluctuating right ptosis, intermittent mild masticatory difficulties (no dyspnea), thin thorax, flat feet
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00057883
0000044535
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00057884
0000051320
breathing difficulty (HP:0002094), feeding difficulty (HP:0011968), ptosis (HP:0000508), no ophthalmoparesis (-HP:0000597), no facial weakness (-HP:0010628), bulbar weakness (HP:0001283), proximal weakness upper limbs (HP:0008997), proximal weakness lower limbs (HP:0008994), distal weakness upper limbs (HP:0008959), distal weakness lower limbs (HP:0009053), axial weakness (HP:0003327), distal-joint laxity (HP:0002761), no contractures (-HP:0001371), no spinal rigidity (-HP:0003306), dysmorphic features (HP:0001999), decrement on RNS (HP:0003403), abnormal jitter (HP:?), lower-respiratory-tract infection (HP:0002783), variation in fiber size (HP:0003557), generalized hypotonia (HP:0001290), gastroesophageal reflux (HP:0002020)
-
-
Familial, autosomal recessive
00y05m
-
00y00m
recurrent apneas (HP:0002104), poor suck (HP:0002033)
-
Jamie Zeegers
00065207
0000051324
feeding difficulty (HP:0011968), ptosis (HP:0000508), no ophthalmoparesis (-HP:0000597), facial weakness (HP:0010628), no bulbar weakness (-HP:0001283), no proximal weakness upper limbs (-HP:0008997), no proximal weakness lower limbs (-HP:0008994), distal weakness upper limbs (HP:0008959), no distal weakness lower limbs (-HP:0009053), right axial weakness (HP:0003327), no distal-joint laxity (-HP:0002761), no contractures (-HP:0001371), spinal rigidity (HP:0003306), dysmorphic features (HP:0001999), mild learning difficulties (HP:0001328), decrement on RNS (HP:0003403), abnormal jitter (HP:?), lower-respiratory-tract infection (HP:0002783), dyspnoea on exertion (HP:0001328), recurrent chest infections (HP:0002783)
-
-
Familial, autosomal recessive
24y
-
00y00m
-
-
Jamie Zeegers
00065215
0000051325
breathing difficulty (HP:0002094), feeding difficulty (HP:0011968), ptosis (HP:0000508), right ophthalmoparesis (HP:0000597), facial weakness (HP:0010628), bulbar weakness (HP:0001283), proximal weakness upper limbs (HP:0008997), proximal weakness lower limbs (HP:0008994), distal weakness upper limbs (HP:0008959), distal weakness lower limbs (HP:0009053), axial weakness (HP:0003327), distal-joint laxity (HP:0002761), no contractures (-HP:0001371), spinal rigidity (HP:0003306), dysmorphic features (HP:0001999), lower-respiratory-tract infection (HP:0002783), chronic lung disease (HP:0006528), hiatus and diaphragmatic hernia (HP:0002036), recurrent chest infection (HP:0002783)
-
-
Familial, autosomal recessive
05y
-
00y00m
severe breathing (HP:0002094) and feeding (HP:0011968) difficulties
-
Jamie Zeegers
00065217
0000058649
unable to work due to general weakness
-
-
Familial, autosomal recessive
-
-
-
-
-
Chun Yiu Law
00078891
0000125696
-
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
-
-
-
-
-
Johan den Dunnen
00152961
0000125697
8y-limb muscle weakness; 10y-scoliosis, able to walk 100 yards, cannot climb stairs unassisted; EMG decremental response on stimulation motor nerves, repetitive compound muscle action potential response to single nerve stimuli; age onset early childhood
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
30y
-
-
ocular muscle weakness
no AChR antibodies
Johan den Dunnen
00152962
0000125698
facial/neck/upper limb weakness, slight difficulty chewing/swallowing, eye movements normal, wasting forearm/hand muscles, no AChR antibodies, single nerve stimuli did not elicit repetitive compound muscle, action potentials
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Isolated (sporadic)
34y
-
14y
lower limb weakness
-
Johan den Dunnen
00152963
0000125699
generalised weakness (sparing extraocular muscles), prominent wasting/weakness finger extensor muscles, atrophy cervical muscles, developed respiratory problems (diaphragmatic weakness), deterioration occurred, no AChR antibodies, single nerve stimuli elicited repetitive compound muscle action potentials
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Isolated (sporadic)
60y
-
16y
generalised weakness
-
Johan den Dunnen
00152964
0000125700
see paper; ..., very extensive over 40 years; generalized myasthenic weakness, mild hand muscle wasting, no AChR antibodies, reacted adversely to anticholinesterase drugs; EMG repetitive muscle response single nerve stimulus
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Isolated (sporadic)
66y
-
23y
arm weakness during pregnancy
-
Johan den Dunnen
00152965
0000125719
7y-intermittent episodes respiratory insufficiency requiring ventilatory support; EMG decremental response on stimulation motor nerves, repetitive compound muscle action potential response to single nerve stimuli; age onset early infancy
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
16y
-
-
myasthenic symptoms
no AChR antibodies
Johan den Dunnen
00152984
0000125720
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Johan den Dunnen
00152985
0000125721
-
syndrome, myasthenic, congenital, slow channel
-
Familial, autosomal recessive
-
-
1d
weak cry
-
Johan den Dunnen
00152986
0000125722
-
syndrome, myasthenic, congenital, slow channel
-
Familial, autosomal recessive
-
-
1d
decreased movements in utero, weak cry and feeble suck
-
Johan den Dunnen
00152987
0000125723
developmental motor milestones normal; 12y-ptosis, limited eye movements, no limb weakness
syndrome, myasthenic, congenital
-
Isolated (sporadic)
12y
-
0d
ptosis, limb muscle weakness
no AChR antibodies
Johan den Dunnen
00152988
0000125724
myasthenic symptoms; 14y normal
syndrome, myasthenic, congenital
-
Isolated (sporadic)
14y
-
0d
ptosis, limb muscle weakness
-
Johan den Dunnen
00152989
0000125725
generalised weakness (sparing extraocular muscles), prominent wasting/weakness finger extensor muscles, deterioration months after pregnancy, no AChR antibodies AChR, single nerve stimuli elicited repetitive compound muscle action potentials; age onset infancy
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Isolated (sporadic)
41y
-
-
-
-
Johan den Dunnen
00152991
0000125726
phenotype compatible with SCCMS
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Isolated (sporadic)
-
-
-
-
-
Angela Abicht
00152992
0000125727
phenotype compatible with SCCMS
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
-
-
-
-
-
Angela Abicht
00152993
0000125728
-
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
-
-
-
-
-
Johan den Dunnen
00152994
0000125729
-
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
-
-
-
-
-
Angela Abicht
00152995
0000125730
-
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
-
-
-
-
-
Angela Abicht
00152996
0000125731
-
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
-
-
-
-
-
Angela Abicht
00152997
0000125734
-
syndrome, myasthenic, congenital, slow channel
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00153006
0000125737
-
syndrome, myasthenic, congenital, slow channel
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00153009
0000125738
global developmental delay, hypotonia, gait problems, weakness
syndrome, myasthenic, congenital
-
Familial, autosomal dominant
-
-
-
-
-
Tom Winder
00153010
0000125762
5y-walking; 8y-ophthalmoparesis; 10y-fatigability; 13y-contractures knee/hip; 13y-loss ambulation; positive edrophonium test
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Isolated (sporadic)
32y
-
0d
poor head control, weak suck
no AChR antibodies
Johan den Dunnen
00153035
0000125763
myasthenic symptoms involving ocular, other cranial and limb muscles; EMG decremental response on stimulation motor nerves, repetitive compound muscle action potential response to single nerve stimuli
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
19y
-
0d
myasthenic symptoms
no AChR antibodies
Johan den Dunnen
00153036
0000125764
EMG decremental response on stimulation motor nerves, partial response to cholinesterase inhibitors
syndrome, myasthenic, congenital
-
Unknown
8y
-
0d
severe myasthenic symptoms requiring ventilation/enteric alimentation
-
Johan den Dunnen
00153037
0000125767
bulbar weakness, scapular winging, scoliosis, hand atrophy
syndrome, myasthenic, congenital
-
Isolated (sporadic)
31y
-
0d
ocular/bulbar/proximal limb weakness
-
Johan den Dunnen
00153045
0000125768
phenotype compatible with adult onset SCCMS
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Familial, autosomal dominant
47y
-
38y
-
-
Angela Abicht
00153046
0000125769
phenotype compatible with adult onset SCCMS
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Familial, autosomal dominant
73y
-
26y
-
-
Angela Abicht
00153047
0000125770
phenotype compatible with early onset SCCMS
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Angela Abicht
00153048
0000125771
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Angela Abicht
00153049
0000125772
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Angela Abicht
00153050
0000125773
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Angela Abicht
00153052
0000125774
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Angela Abicht
00153053
0000125775
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Angela Abicht
00153055
0000125776
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Angela Abicht
00153056
0000125777
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Tom Winder
00153061
0000125779
myasthenic symptoms involving ocular, other cranial and limb muscles; EMG decremental response on stimulation motor nerves, repetitive compound muscle action potential response to single nerve stimuli
syndrome, myasthenic, congenital, slow channel (SCCMS)
-
Unknown
19y
-
0d
myasthenic symptoms
no AChR antibodies
Johan den Dunnen
00153063
0000125780
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
6y
-
-
-
-
Johan den Dunnen
00153064
0000125781
9y-loss ambulation
syndrome, myasthenic, congenital
-
Isolated (sporadic)
15y
-
1m
floppy, head control
-
Johan den Dunnen
00153065
0000125782
post-partum difficulties feeding, sucking with frequent chokes; neonatal left-side eyelid ptosis, facial weakness, daytime-dependent abnormal fatigue, muscular hypotonia; motor development delayed
syndrome, myasthenic, congenital
-
Isolated (sporadic)
7y
-
0d
-
-
Angela Abicht
00153066
0000125785
no anti-AChR antibodies
syndrome, myasthenic, congenital
-
Unknown
20y
-
0d
myasthenic symptoms
-
Johan den Dunnen
00153069
0000125786
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00153070
0000125787
-
syndrome, myasthenic, congenital
-
Familial, autosomal dominant
-
-
-
-
-
Angela Abicht
00153071
0000125788
early onset severe CMS with contractures
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153072
0000125789
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Johan den Dunnen
00153073
0000125790
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00153074
0000125791
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00153075
0000125792
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Johan den Dunnen
00153078
0000125793
bilateral ptosis, strabismus, hyperlordosis, foot drop.
syndrome, myasthenic, congenital
-
Familial, autosomal dominant
-
-
-
-
type 1 fiber predominance seen in muscle biopsy.
Tom Winder
00153083
0000125794
profound muscle weakness; ventilator-dependent since birth; improves with Mestinin
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Tom Winder
00153084
0000125801
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Johan den Dunnen
00153090
0000125803
-
syndrome, myasthenic, congenital
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00153092
0000125805
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00153094
0000125811
-
syndrome, myasthenic, congenital
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00153100
0000125812
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Johan den Dunnen
00153101
0000125813
-
syndrome, myasthenic, congenital
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00153102
0000125814
-
syndrome, myasthenic, congenital
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00153103
0000125831
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Johan den Dunnen
00153120
0000125832
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Johan den Dunnen
00153121
0000125833
-
syndrome, myasthenic, congenital
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00153122
0000125855
-
syndrome, myasthenic, congenital
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00153144
0000125861
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00153150
0000125862
-
syndrome, myasthenic, congenital
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00153151
0000125864
-
syndrome, myasthenic, congenital
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00153153
0000125870
-
syndrome, myasthenic, congenital
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00153159
0000125871
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Tom Winder
00153162
0000125872
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Tom Winder
00153163
0000125873
congenital ptosis, ophthalmoplegia
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Tom Winder
00153164
0000125874
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Tom Winder
00153165
0000125875
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Johan den Dunnen
00153167
0000125876
ptosis, limited eye movements, mild facial/limb weakness; 36y-marked bilateral ptosis, severe bilateral reduction eye abduction, fatigable weakness (more proximal then distal limb muscles); age onset early childhood
syndrome, myasthenic, congenital
-
Isolated (sporadic)
36y
-
-
myasthenic symptoms
no AChR antibodies
Angela Abicht
00153171
0000125877
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153174
0000125878
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153175
0000125879
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153176
0000125880
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153177
0000125881
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153178
0000125882
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153179
0000125883
-
syndrome, myasthenic, congenital, fast channel
-
Unknown
-
-
-
-
-
Angela Abicht
00153180
0000125884
-
syndrome, myasthenic, congenital, fast channel
-
Unknown
-
-
-
-
-
Angela Abicht
00153181
0000125885
-
syndrome, myasthenic, congenital, fast channel
-
Unknown
-
-
-
-
-
Angela Abicht
00153182
0000125886
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153183
0000125887
-
syndrome, myasthenic, congenital
-
Unknown
-
-
<1y
-
-
Angela Abicht
00153184
0000125888
-
syndrome, myasthenic, congenital
-
Unknown
-
-
<1y
-
-
Angela Abicht
00153185
0000125889
-
syndrome, myasthenic, congenital
-
Unknown
-
-
<1y
-
-
Angela Abicht
00153187
0000125890
-
syndrome, myasthenic, congenital
-
Unknown
-
-
<1y
-
-
Angela Abicht
00153188
0000125891
-
syndrome, myasthenic, congenital
-
Unknown
-
-
<1y
-
-
Angela Abicht
00153189
0000125892
-
syndrome, myasthenic, congenital
-
Unknown
-
-
<1y
-
-
Angela Abicht
00153190
0000125893
-
syndrome, myasthenic, congenital
-
Unknown
-
-
<1y
-
-
Angela Abicht
00153191
0000125894
-
syndrome, myasthenic, congenital
-
Unknown
-
-
<1y
-
-
Angela Abicht
00153192
0000125895
-
syndrome, myasthenic, congenital
-
Unknown
-
-
<1y
-
-
Angela Abicht
00153193
0000125896
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153194
0000125897
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153195
0000125898
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153196
0000125899
-
syndrome, myasthenic, congenital
-
Unknown
-
-
-
-
-
Angela Abicht
00153197
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