Phenotypes for disease #04422 (BTHLM2 (myopathy, Bethlem, type 2 (BTHLM-2)), OMIM:616471)

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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     
0000345871 Motor delay (HP:0001270); neonatal hypotonia (HP:0001319); decreased fetal movement (HP:0001558); intrauterine growth retardation (HP:0001511); oligohydramnios (HP:0001562); high, narrow palate (HP:0002705); hyperextensible skin (HP:0000974); palmoplantar cutis laxa (HP:0007517); pectus excavatum (HP:0000767); neck muscle weakness (HP:0000467); kyphoscoliosis (HP:0002751); bilateral knee contractures (HP:0034671); distal joint hypermobility (HP:0020152); respiratory insufficiency due to muscle weakness (HP:0002747); pelvic girdle muscle atrophy (HP:0008988); proximal lower limb amyotrophy (HP:0008956); distal lower limb amyotrophy (HP:0008944); soft, doughy skin (HP:0001027). ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1A/1B; UCMD1A/1B EHLERS-DANLOS SYNDROME, MYOPATHIC TYPE; EDSMYP Familial, autosomal recessive 00y23m 00y23m 00y Neonatal hypotonia (HP:0001319) deepsubs Deepak Subramanian 00457407
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