Disease #01963 (NEM2 (myopathy, nemaline, type 2 (NEM2)), OMIM:256030)

Official abbreviation NEM2
Name myopathy, nemaline, type 2 (NEM2)
OMIM ID 256030
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 11
Phenotype entries for this disease 11
Associated with 1 gene NEB
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-09-30 10:59:30 +02:00 (CEST)


Individuals

11 entries on 1 page. Showing entries 1 - 11.
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00314966 01-001 PubMed: Laflamme 2021 6-generation family, 1 affected M yes Algeria - - - - - NEM2 Myopathy - NEB 1 1 Baiba Lace
00419096 - PubMed: Sagath 2025 - M no (Canada) - - - - - NEM2 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. NEB NEB 2 2 Lydia Sagath
00426479 - - index case unaffected heterozygous parents F no Paraguay - - - - - NEM2 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 - NEB 2 1 María Eugenia Foncuberta
00436931 - PubMed: Sagath 2025 - F ? New Zealand Maori ? - - - NEM2 neonatal hypotonia (HP:0001319); reduced tendon reflexes (HP:0001315); proximal muscle weakness (HP:0003701) NEB NEB 3 1 Lydia Sagath
00437018 - PubMed: Sagath 2025 - M no (Australia) Pakistani - - - - NEM2 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) - NEB 2 1 Lydia Sagath
00441137 - PubMed: Sagath 2025 - - ? (United States) - - - - - NEM2 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) NEB NEB 2 1 Lydia Sagath
00448476 - PubMed: Sagath 2025 - M no United Kingdom (Great Britain) - - - - - NEM2 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) NEB NEB 2 1 Lydia Sagath
00448477 - PubMed: Sagath 2025 - M no United Kingdom (Great Britain) - - - - - NEM2 delayed speech and language development (HP:0000750); hypotonia (HP:0001252); high palate (HP:0000218); decreased fetal movement (HP:0001558) NEB NEB 2 1 Lydia Sagath
00448478 - PubMed: Sagath 2025 - F yes (United States) - - - - - NEM2 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) NEB NEB 1 1 Lydia Sagath
00452781 - PubMed: Sagath 2025 - - no - - - - - - NEM2 - NEB NEB 2 1 Lydia Sagath
00464362 - - - - - - - - - - - NEM2 - NEB NEB 2 1 Min Peng
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