Tetany

Symptom Information:

Symptom ID: HPO:0001281
Synonyms:
Tetanus (disorder) [Orphanet:44200]
Tetany (disorder) [Orphanet:44200]
Tetanus [Orphanet:44200]
Tetany [Orphanet:44200]
Tetany [OMIM:Tetany]
Contractures/cramps/trismus/tetania/claudication/opisthotonos [Orphanet:44200]
Tetany [MedDRA:10043380]
Carpo-pedal spasm [MedDRA:10043380]
Generalised tetany [MedDRA:10043380]
Hypocalcemic tetany [MedDRA:10043380]
Spasm carpopedal [MedDRA:10043380]
Tetany hypocalcemic [MedDRA:10043380]
Accoucheur's hand [MedDRA:10043380]
Hyperventilation tetany [MedDRA:10043380]
Hypocalcaemic tetany [MedDRA:10043380]
Tetany hypocalcaemic [MedDRA:10043380]
Generalized tetany [MedDRA:10043380]
Tetanus [MedDRA:10043376]
Clostridium tetani infection [MedDRA:10043376]
Tetanus like [MedDRA:10043376]
Tetanus-like [MedDRA:10043376]
Carpopedal spasm [OMIM:Carpopedal spasm]
Muscle spasms [MedDRA:10028334]
Muscle contracture [Orphanet:44200]
Contracture (morphologic abnormality) [Orphanet:44200]
Spasm (finding) [Orphanet:44200]
Muscle contracture (disorder) [Orphanet:44200]
Contracture [Orphanet:44200]
Spasm [Orphanet:44200]
Quality:
Cross references:
Orphanet:44200 "Contractures/cramps/trismus/tetania/claudication/opisthotonos" [Orphanet:44200]
OMIM: "Tetany" [OMIM:Tetany]
OMIM: "Carpopedal spasm" [OMIM:Carpopedal spasm]
UMLS:C0039621 "Tetany" [HPO:0001281]
UMLS:C0039614 "Tetanus" [Orphanet:44200]
UMLS:C0039621 "Tetany" [Orphanet:44200]
UMLS:C0009917 "Contracture" [Orphanet:44200]
UMLS:C0037763 "Spasm" [Orphanet:44200]
Is a (Direct Parents):
Orphanet Muscle anomalies
MedDRA Muscle related signs and symptoms NEC
MedDRA Abnormal muscle tone
HPO         Abnormality of muscle physiology
Orphanet Trismus
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:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Muscle disorders(MedDRA:10028302)
       Muscle related signs and symptoms NEC(MedDRA:10028326)
          Tetany(HPO:0001281)
Nervous system disorders(MedDRA:10029205)
    Neuromuscular disorders(MedDRA:10029317)
       Abnormal muscle tone(HPO:0003808)
          Tetany(HPO:0001281)
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)