Infantile axial hypotonia
Symptom Information:
Symptom ID: | HPO:0009062 | ||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Abnormal muscle tone(HPO:0003808) Muscular hypotonia(HPO:0001252) Muscular hypotonia of the trunk(HPO:0008936) Infantile axial hypotonia(HPO:0009062) Infantile muscular hypotonia(HPO:0008947) Infantile axial hypotonia(HPO:0009062) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome | (Orphanet:85295) |