Generalized neonatal hypotonia
Symptom Information:
Symptom ID: | HPO:0008935 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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) Neonatal hypotonia(HPO:0001319) Generalized neonatal hypotonia(HPO:0008935) MedDRA: |
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Database Frequency: | 9 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Combined oxidative phosphorylation defect type 4 | (Orphanet:254925) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED | (OMIM:300580) |
PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER) | (OMIM:614882) |
PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER) | (OMIM:614859) |
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER) | (OMIM:614862) |
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) | (OMIM:614866) |
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER) | (OMIM:614870) |
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER) | (OMIM:614872) |
PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER) | (OMIM:614876) |