Central hypotonia
Symptom Information:
Symptom ID: | HPO:0011398 | ||
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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of central motor function(HPO:0011442) Central hypotonia(HPO:0011398) MedDRA: |
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Database Frequency: | 12 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Cataract-congenital heart disease-neural tube defect syndrome | (Orphanet:314993) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15 | (OMIM:615006) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Intellectual deficit, X-linked, Kroes type | (Orphanet:163961) |
Joubert syndrome 5 | (OMIM:610188) |
KABUKI SYNDROME 2 | (OMIM:300867) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
PEROXISOME BIOGENESIS DISORDER 11B | (OMIM:614885) |
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) | (OMIM:614886) |
PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) | (OMIM:614887) |
Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |