Phenotypes for disease #02383 (DA2B1 (arthrogryposis, distal, type 2B1a), OMIM:601680)

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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     
0000357042 Congenital myastenic syndrome, Neck muscle weakness, Ptosis, Dysphagia, Poor suck, Sudden episodic apnea, Fatigable weakness, Proximal muscle weakness, Frontalis muscle weakness, Intermittent episodes of respiratory insufficiency due to muscle weakness, Feeding difficulties, Decreased fetal movement, Difficulty walking, Easy fatigability, Spinal deformities, Motor delay, Dysphonia, Kyphoscoliosis, Spinal rigidity, Stridor, Low-set ears, Gastroesophageal reflux Congenital myastenic syndrome Arthrogryposis, distal Isolated (sporadic) - - - - - Camille Verebi 00472233
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