skin disease +
inherited metabolic disorder +
amyloidosis +

aceruloplasminemia
Achenbach syndrome
adermatoglyphia
amino acid metabolic disorder +
ancylostomiasis
angioedema +
apolipoprotein A-IV associated amyloidosis
aromatic L-amino acid decarboxylase deficiency
autoimmune disease of skin and connective tissue +
bilirubin metabolic disorder +
Birt-Hogg-Dube syndrome
Brooke-Spiegler syndrome
carbohydrate metabolic disorder +
cellulitis +
cercarial dermatitis
cerebral amyloid angiopathy +
cerebral amyloid angiopathy +
chancroid
cherubism
chronic mucocutaneous candidiasis
chronic ulcer of skin +
coenurosis
contagious pustular dermatitis
cutaneous anthrax
cutaneous candidiasis
cutaneous leishmaniasis
cutaneous lupus erythematosus +
cutaneous mastocytosis +
cutaneous porphyria
cutis laxa +
cysticercosis
D-glyceric aciduria
dermatitis +
dermatomycosis +
dermatomyositis +
dialysis-related amyloidosis
dioctophymiasis
dipetalonemiasis
dirofilariasis
dopamine beta-hydroxylase deficiency
dyskeratosis congenita +
eczema herpeticum
epidermal nevus
erythema multiforme
erythematosquamous dermatosis
erythrokeratodermia variabilis +
exanthem +
eyelid disease +
facial dermatosis
familial hypocalciuric hypercalcemia +
familial progressive hyperpigmentation with or without hypopigmentation
familial visceral amyloidosis
familial visceral amyloidosis
filarial elephantiasis
glycerol kinase deficiency
Gordon Holmes syndrome
granulomatosis with polyangiitis
Greenberg dysplasia
hand dermatosis
hemorrhoid +
HRPT-related hyperuricemia
hyperphosphatemic familial tumoral calcinosis
hypomelanosis of Ito
ichthyosis +
immunoglobulin heavy chain amyloidosis
immunoglobulin heavy-and-light chain
immunoglobulin light chain amyloidosis
immunoglobulin light chain amyloidosis
inflammatory poikiloderma with hair abnormalities and acral keratoses
isolated elevated serum creatine phosphokinase levels
isolated hyperchlorhidrosis
isolated sulfite oxidase deficiency
keratosis +
Kimura disease
Kindler syndrome
large congenital melanocytic nevus
leg dermatosis
lichen disease +
lipid metabolism disorder +
lipomatosis +
loiasis
lysosomal storage disease +
mansonelliasis
metal metabolism disorder +
mitochondrial metabolism disease +
mongolian spot
multiple acyl-CoA dehydrogenase deficiency
multiple benign circumferential skin creases on limbs +
multiple cutaneous and mucosal venous malformations
necrobiosis lipoidica
Netherton syndrome
nonsyndromic aplasia cutis congenita
panniculitis +
peeling skin syndrome +
peroxisomal disease +
phosphoribosylpyrophosphate synthetase superactivity
pigmentation disease +
pityriasis rubra pilaris
PLACK syndrome
plasma protein metabolism disease +
poikiloderma with neutropenia
porphyria +
purine-pyrimidine metabolic disorder +
pyrimidine metabolic disorder +
reactive cutaneous fibrous lesion +
restrictive dermopathy +
Ritter's disease
rosacea
Rothmund-Thomson syndrome
scalp dermatosis
scleredema adultorum
sebaceous gland disease +
serum amyloid A amyloidosis
skin atrophy
skin benign neoplasm +
skin cancer +
skin carcinoma in situ
skin sarcoidosis
smallpox +
Stevens-Johnson syndrome
stiff skin syndrome
strongyloidiasis
sweat gland disease +
Sweet syndrome
thiopurine S-methyltransferase deficiency
tinea barbae
tinea corporis +
tinea manuum
tinea pedis
transthyretin amyloidosis
transthyretin amyloidosis
trimethylaminuria
tyrosinemia type II
urticaria +
UV-sensitive syndrome
variant ABeta2M amyloidosis
variant ABeta2M amyloidosis
vascular skin disease
verruciform xanthoma of skin
vitamin metabolic disorder +
warfarin resistance
warfarin sensitivity
white sponge nevus +
wild-type amyloidosis
X-linked warfarin sensitivity
yellow nail syndrome

Finnish type amyloidosis
primary localized cutaneous amyloidosis 1
primary localized cutaneous amyloidosis 2
primary localized cutaneous amyloidosis 3