Symptom Information: Sort according to HPO 

1
 (HPO:0001025) Urticaria Very frequent [Orphanet] 73 / 7739
2
 (HPO:0000989) Pruritus Very frequent [Orphanet] 111 / 7739
3
 (HPO:0003326) Myalgia Very frequent [Orphanet] 143 / 7739
4
 (HPO:0000509) Conjunctivitis 47 / 7739
5
 (HPO:0005059) Arthralgia/arthritis Very frequent [Orphanet] 141 / 7739
6
 (HPO:0100769) Synovitis Very frequent [Orphanet] 86 / 7739
7
 (HPO:0002315) Headache Frequent [Orphanet] 175 / 7739
8
 (HPO:0001944) Dehydration Occasional [Orphanet] 59 / 7739
9
 (HPO:0002017) Nausea and vomiting Frequent [Orphanet] 134 / 7739
10
 (HPO:0000407) Sensorineural hearing impairment Occasional [Orphanet] 524 / 7739
11
 (HPO:0001945) Fever Very frequent [Orphanet] 218 / 7739
12
 (HPO:0001917) Renal amyloidosis rare [HPO:probinson] 8 / 7739
13
 (HPO:0001933) Subcutaneous hemorrhage Very frequent [Orphanet] 50 / 7739
14
 (HPO:0001954) Episodic fever 27 / 7739
15
 (HPO:0001974) Leukocytosis 33 / 7739
16
 (OMIM) Renal amyloidosis, late-onset 2 / 7739
17
 (OMIM) Arthralgia, episodic 2 / 7739
18
 (OMIM) Maculopapular rash, episodic 2 / 7739
19
 (OMIM) Rash may or may not be pruritic 2 / 7739
20
 (OMIM) Episodic myalgia 3 / 7739
21
 (OMIM) Swelling of the extremities, episodic 1 / 7739
22
 (OMIM) Headache, episodic 1 / 7739
23
 (OMIM) Polymorphonuclear leukocytosis, episodic 2 / 7739
24
 (OMIM) Increased serum C-reactive protein, episodic 1 / 7739
25
 (HPO:0001357) Plagiocephaly Very frequent [Orphanet] 106 / 7739
26
 (HPO:0001324) Muscle weakness Very frequent [Orphanet] 859 / 7739
27
 (HPO:0100533) Inflammatory abnormality of the eye Occasional [Orphanet] 70 / 7739
28
 (HPO:0030350) Erythematous papule Very frequent [Orphanet] 123 / 7739
29
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
30
 (HPO:0002829) Arthralgia 79 / 7739
31
 (HPO:0003593) Infantile onset 249 / 7739