Episodic fever
Symptom Information:
Symptom ID: | HPO:0001954 | ||||||
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) Fever(HPO:0001945) Episodic fever(HPO:0001954) MedDRA: |
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Database Frequency: | 27 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
COLD-INDUCED SWEATING SYNDROME 1 | (OMIM:272430) |
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY | (OMIM:203400) |
Cold-induced sweating syndrome | (Orphanet:157820) |
Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
Combined immunodeficiency due to ORAI1 deficiency | (Orphanet:317428) |
Combined immunodeficiency due to STIM1 deficiency | (Orphanet:317430) |
Dihydropteridine reductase deficiency | (Orphanet:226) |
FAMILIAL MEDITERRANEAN FEVER | (OMIM:249100) |
FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT | (OMIM:134610) |
Familial Mediterranean fever | (Orphanet:342) |
Familial cold urticaria | (Orphanet:47045) |
Familial dysautonomia | (Orphanet:1764) |
Familial hypoaldosteronism | (Orphanet:427) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5 | (OMIM:613101) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
Hereditary sensory and autonomic neuropathy type 5 | (Orphanet:64752) |
Idiopathic recurrent pericarditis | (Orphanet:251307) |
Isolated agammaglobulinemia | (Orphanet:229717) |
Krabbe disease | (Orphanet:487) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Muckle-Wells syndrome | (Orphanet:575) |
NLRP12-associated hereditary periodic fever syndrome | (Orphanet:247868) |
PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN | (OMIM:260570) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
TRAPS syndrome | (Orphanet:32960) |