Phenotypes for disease #01963 (NEM2 (myopathy, nemaline, type 2 (NEM2)), OMIM:256030)

11 entries on 1 page. Showing entries 1 - 11.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

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Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000238718 Myopathy - - Familial, autosomal recessive 06y - - - - Baiba Lace 00314966
0000310384 Hypotonia (HP:0001252) since birth; classical myopathic facies (HP:0002058); proximal muscle weakness (HP:0003701) with mild respiratory involvement; EGM: myopathic abnormalities (HP:0003458); normal CK. Unspecified congenital myopathy NEM2 Familial, autosomal recessive - - - - - Lydia Sagath 00419096
0000317633 HP:0001290 Generalized hypotonia HP:0001270 Motor delay HP:0003327 Axial muscle weakness HP:0003325 Limb-girdle muscle weakness (shoulder girdles predominance) HP:0003307 Hyperlordosis - NEM2 Familial, autosomal recessive - - - - - María Eugenia Foncuberta 00426479
0000326933 neonatal hypotonia (HP:0001319); reduced tendon reflexes (HP:0001315); proximal muscle weakness (HP:0003701) Nemaline myopathy Nemaline myopathy Familial, autosomal recessive 01y - - - - Lydia Sagath 00436931
0000326938 proximal muscle weakness (HP:0003701); weakness of facial muscles (HP:0030319); reduced tendon reflexes (HP:0001315); delayed motor milestones (HP:0001270); hypotonia (HP:0001252); speech articulation difficulties (HP:0009088); dysarthria (HP:0001260) 0y - Familial, autosomal recessive 04y - 00y - - Lydia Sagath 00437018
0000327676 areflexia (HP:0001284); weakness of facial musculature (HP:0030319); proximal muscle weakness (HP:0003701) Nemaline myopathy NEM2 Familial, autosomal recessive 7 - - - - Lydia Sagath 00437767
0000330576 neonatal hypotonia (HP:0001319); multiple prenatal fractures (HP:0005855); neonatal respiratory distress (HP:0002643); respiratory insufficiency due to muscle weakness (HP:0002747); feeding difficulties in infancy (HP:0008872); gastroesophageal reflux (HP:0002020); choking episodes (HP:0030842); delayed motor milestones (HP:0001270); type 1 muscle fiber predominance (HP:0003803); abnormality of skeletal muscle fiber size (HP:0012084) NEM2 NEM2 Unknown - - - - - Lydia Sagath 00441137
0000337664 neonatal hypotonia (HP:0001319); neonatal respiratory distress (HP:0002643); feeding difficulties in infancy (HP:0008872); scoliosis (HP:0002650); proximal muscle weakness (HP:0003701); EMG abnormality (HP:0003457);type 2 muscle fiber predominance (HP:0010602); abnormality of skeletal muscle fiber size (HP:0012084) - NEM2 Familial, autosomal recessive - - - - - Lydia Sagath 00448476
0000337665 delayed speech and language development (HP:0000750); hypotonia (HP:0001252); high palate (HP:0000218); decreased fetal movement (HP:0001558) - NEM2 Familial, autosomal recessive - - - - - Lydia Sagath 00448477
0000337666 neonatal hypotonia (HP:0001319); lower limb muscle weakness (HP:0007340); prominent nose (HP:0000448); pes cavus (HP:0001761); hepatomegaly (HP:0002240); neonatal respiratory distress (HP:0002643); feeding difficulties in infancy (HP:0008872); delayed motor milestones (HP:0001270); failure to thrive (HP:0001508); areflexia (HP:0001284); dysarthria (HP:0001260); proximal muscle weakness (HP:0003701); type 1 muscle fiber predominance (HP:0003803); abnormality of skeletal muscle fiber size (HP:0012084) - NEM2 Familial, autosomal recessive - - - - - Lydia Sagath 00448478
0000341353 - NEM2 NEM2 Familial, autosomal recessive - - - - - Lydia Sagath 00452781
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