Limb hypertonia
Symptom Information:
Symptom ID: | HPO:0002509 | ||||
Synonyms: |
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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) Abnormal pyramidal signs(HPO:0007256) Hypertonia(HPO:0001276) Limb hypertonia(HPO:0002509) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Limb hypertonia(HPO:0002509) MedDRA: |
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Database Frequency: | 13 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Amish lethal microcephaly | (Orphanet:99742) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21 | (OMIM:615918) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Dihydropteridine reductase deficiency | (Orphanet:226) |
Familial dyskinesia and facial myokymia | (Orphanet:324588) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
Gaucher disease type 2 | (Orphanet:77260) |
LISSENCEPHALY 6 WITH MICROCEPHALY | (OMIM:616212) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2B | (OMIM:612389) |
Propionic acidemia | (Orphanet:35) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |