Tetany
Symptom Information:
Symptom ID: | HPO:0001281 | |||||||||||||||||||||||||||||
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 musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Tetany(HPO:0001281) MedDRA: Nervous system disorders(MedDRA:10029205) Neuromuscular disorders(MedDRA:10029317) Abnormal muscle tone(HPO:0003808) Tetany(HPO:0001281) Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle related signs and symptoms NEC(MedDRA:10028326) Tetany(HPO:0001281) |
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Database Frequency: | 20 / 7739 | |||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Autosomal recessive primary hypomagnesemia with normocalcuria and hypocalcemia | (Orphanet:30924) |
BARTTER SYNDROME, ANTENATAL, TYPE 1 | (OMIM:601678) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
Bartter syndrome | (Orphanet:112) |
Bartter syndrome with hypocalcemia | (Orphanet:263417) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
DIGEORGE SYNDROME | (OMIM:188400) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis | (Orphanet:31043) |
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland | (Orphanet:2239) |
Familial isolated hypoparathyroidism due to impaired PTH secretion | (Orphanet:189466) |
Gitelman syndrome | (Orphanet:358) |
HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES | (OMIM:239350) |
HYPOCALCEMIA, AUTOSOMAL DOMINANT 2 | (OMIM:615361) |
MELAS | (Orphanet:550) |
Pearson syndrome | (Orphanet:699) |
Sanjad-Sakati syndrome | (Orphanet:2323) |