HP:0000007 | Autosomal recessive inheritance | "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators] |
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HP:0001265 | Hyporeflexia | |
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HP:0001284 | Areflexia | |
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HP:0001308 | Tongue fasciculations | |
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HP:0001324 | Muscle weakness | "Reduced strength of muscles." [HPO:curators] |
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HP:0001558 | Decreased fetal movement | "An abnormal reduction in quantity or strength of fetal movements." [HPO:curators] |
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HP:0001629 | Ventricular septal defect | "A hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the most superior aspect of the ventricular septum." [HPO:curators] |
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HP:0001631 | Atrial septal defect | "Atrial septal defect (ASD) is a congenital heart defect that enables blood flow between the left and right atria via the interatrial septum. The three common types of ASD are sinus venosus defects, ostium secundum defects, and ostium primum defects." [HPO:curators] |
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HP:0002093 | Respiratory insufficiency | |
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HP:0002205 | Recurrent respiratory infections | |
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HP:0002378 | Hand tremor | |
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HP:0002398 | Degeneration of anterior horn cells | |
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HP:0002522 | Areflexia in lower limbs | |
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HP:0002878 | Early respiratory failure | |
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HP:0003394 | Muscle cramps | |
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HP:0003445 | EMG shows neuropathic changes | |
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HP:0003457 | Abnormal EMG findings | "Abnormal results of investigations using electromyography (EMG)." [HPO:curators] |
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HP:0003581 | Onset in adulthood | |
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HP:0003676 | Progressive disorder | |
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HP:0003677 | Slow progression | |
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HP:0003701 | Proximal muscle weakness | "A lack of strength of the proximal muscles." [HPO:curators] |
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HP:0007126 | Proximal amyotrophy | "Amyotrophy (muscular atrophy) affecting the proximal musculature." [HPO:curators] |
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HP:0007269 | Spinal muscular atrophy | "Muscular weakness and atrophy related to loss of the motor neurons of the spinal cord and brainstem." [HPO:curators] |
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HP:0007289 | Limb fasciculations | "Fasciculations affecting the musculature of the arms and legs." [HPO:curators] |
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HP:0008994 | Proximal muscle weakness in lower limbs | "A lack of strength of the proximal muscles of the legs." [HPO:curators] |
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