Malignant hyperthermia
Symptom Information:
Symptom ID: | HPO:0002047 | ||||||||||||||
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 metabolism/homeostasis(HPO:0001939) Abnormality of temperature regulation(HPO:0004370) Malignant hyperthermia(HPO:0002047) MedDRA: General disorders and administration site conditions(MedDRA:10018065) Body temperature conditions(MedDRA:10005908) Body temperature altered(MedDRA:10005907) Malignant hyperthermia(HPO:0002047) |
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Database Frequency: | 20 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
ARTHROGRYPOSIS, DISTAL, TYPE 2A | (OMIM:193700) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Familial dysautonomia | (Orphanet:1764) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
Harlequin ichthyosis | (Orphanet:457) |
Hyperkalemic periodic paralysis | (Orphanet:682) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2 | (OMIM:154275) |
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3 | (OMIM:154276) |
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 4 | (OMIM:600467) |
Malignant hyperthermia | (Orphanet:423) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Moderate multiminicore disease with hand involvement | (Orphanet:178145) |
Native American myopathy | (Orphanet:168572) |
PGM1-CDG | (Orphanet:319646) |
Schwartz-Jampel syndrome | (Orphanet:800) |
X-linked lethal multiple pterygium syndrome | (Orphanet:79447) |
Yellow fever | (Orphanet:99829) |