Phenotypes for disease #05618 (NMD (neuromuscular disorder (NMD)))

469 entries on 5 pages. Showing entries 1 - 100.
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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
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