Episodic fever

Symptom Information:

Symptom ID: HPO:0001954
Synonyms:
Hyperthermia, episodic [HPO:0001954]
Increased body temperature, episodic [HPO:0001954]
Intermittent fever [HPO:0001954]
Hyperthermia, episodic [OMIM:Hyperthermia, episodic]
Intermittent fever [OMIM:Intermittent fever]
Fever, episodic [OMIM:Fever, episodic]
Quality:
Cross references:
OMIM: "Hyperthermia, episodic" [OMIM:Hyperthermia, episodic]
OMIM: "Intermittent fever" [OMIM:Intermittent fever]
OMIM: "Fever, episodic" [OMIM:Fever, episodic]
Is a (Direct Parents):
HPO         Fever
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:
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)