Phenotypes for disease #00328 (CCD (central core disease (CCD)), OMIM:117000)

147 entries on 2 pages. Showing entries 1 - 100.
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AscendingPhenotype 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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