|
1p36 deletion syndrome
|
(Orphanet:1606)
|
|
Aggressive systemic mastocytosis
|
(Orphanet:98850)
|
|
Angioma serpiginosum
|
(Orphanet:95429)
|
|
Bannayan-Riley-Ruvalcaba syndrome
|
(Orphanet:109)
|
|
Blau syndrome
|
(Orphanet:90340)
|
|
Bullous pemphigoid
|
(Orphanet:703)
|
|
Chronic granulomatous disease
|
(Orphanet:379)
|
|
Congenital toxoplasmosis
|
(Orphanet:858)
|
|
Cowden syndrome
|
(Orphanet:201)
|
|
Cutaneous lupus erythematosus
|
(Orphanet:535)
|
|
Cutaneous mastocytoma
|
(Orphanet:79455)
|
|
Cutaneous mastocytosis
|
(Orphanet:66646)
|
|
Darier disease
|
(Orphanet:218)
|
|
Dermatitis herpetiformis
|
(Orphanet:1656)
|
|
Drug rash with eosinophilia and systemic symptoms
|
(Orphanet:139402)
|
|
Dyschromatosis symmetrica hereditaria
|
(Orphanet:41)
|
|
Dyschromatosis universalis
|
(Orphanet:241)
|
|
Dyskeratosis congenita
|
(Orphanet:1775)
|
|
Ebola hemorrhagic fever
|
(Orphanet:319218)
|
|
Ehlers-Danlos syndrome, vascular type
|
(Orphanet:286)
|
|
Eosinophilic fasciitis
|
(Orphanet:3165)
|
|
Erythrokeratodermia - ataxia
|
(Orphanet:1955)
|
|
Erythrokeratodermia variabilis
|
(Orphanet:317)
|
|
Exostoses - anetodermia - brachydactyly type E
|
(Orphanet:1962)
|
|
Familial multiple nevi flammei
|
(Orphanet:624)
|
|
Focal dermal hypoplasia
|
(Orphanet:2092)
|
|
Hairy cell leukemia variant
|
(Orphanet:300878)
|
|
Hashimoto-Pritzker syndrome
|
(Orphanet:99872)
|
|
Hennekam-Beemer syndrome
|
(Orphanet:2135)
|
|
Hypo- and hypermelanotic cutaneous macules - retarded growth - intellectual deficiency
|
(Orphanet:2435)
|
|
Immunoglobulin A vasculitis
|
(Orphanet:761)
|
|
KID syndrome
|
(Orphanet:477)
|
|
Lyell syndrome
|
(Orphanet:537)
|
|
Lyme disease
|
(Orphanet:91546)
|
|
Lymphangioleiomyomatosis
|
(Orphanet:538)
|
|
Maculopapular cutaneous mastocytosis
|
(Orphanet:79457)
|
|
Mastocytosis
|
(Orphanet:98292)
|
|
Megalencephaly-capillary malformation-polymicrogyria syndrome
|
(Orphanet:60040)
|
|
Neurofibromatosis type 1
|
(Orphanet:636)
|
|
PTEN hamartoma tumor syndrome
|
(Orphanet:306498)
|
|
Peutz-Jeghers syndrome
|
(Orphanet:2869)
|
|
Piebald trait - neurologic defects
|
(Orphanet:2885)
|
|
Piebaldism
|
(Orphanet:2884)
|
|
Primary cutaneous lymphoma
|
(Orphanet:542)
|
|
Progressive osseous heteroplasia
|
(Orphanet:2762)
|
|
Relapsing polychondritis
|
(Orphanet:728)
|
|
Rheumatic fever
|
(Orphanet:3099)
|
|
Scrub typhus
|
(Orphanet:83317)
|
|
Steatocystoma multiplex - natal teeth
|
(Orphanet:3184)
|
|
Stevens-Johnson syndrome
|
(Orphanet:36426)
|
|
Sweet syndrome
|
(Orphanet:3243)
|
|
TRAPS syndrome
|
(Orphanet:32960)
|
|
Tuberous sclerosis
|
(Orphanet:805)
|
|
Typhoid
|
(Orphanet:99745)
|
|
Xeroderma pigmentosum
|
(Orphanet:910)
|