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
chronic mucocutaneous candidiasis
chronic ulcer of skin +
coenurosis
contagious pustular dermatitis
contractures, pterygia, and spondylocarpotarsal fusion syndrome +
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 +
immunodeficiency 130
immunoglobulin heavy chain amyloidosis
immunoglobulin heavy-and-light chain
immunoglobulin light chain amyloidosis
immunoglobulin light chain amyloidosis
infantile hypercalcemia 1
infantile hypercalcemia 2
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
poor metabolism of thiopurines +
porphyria +
Pthirus pubis infestation
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
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