skin disease +
digenic disease +

Achenbach syndrome
acrocallosal syndrome
adermatoglyphia
AMED syndrome
ancylostomiasis
angioedema +
autoimmune disease of skin and connective tissue +
autosomal recessive nonsyndromic deafness 1A
autosomal-mitochondrial sensorineural deafness
Birt-Hogg-Dube syndrome
Brooke-Spiegler syndrome
cellulitis +
cercarial dermatitis
chancroid
cherubism
chronic mucocutaneous candidiasis
chronic ulcer of skin +
coenurosis
contagious pustular dermatitis
contractures, pterygia, and spondylocarpotarsal fusion syndrome +
craniosynostosis 7
cutaneous anthrax
cutaneous candidiasis
cutaneous leishmaniasis
cutaneous lupus erythematosus +
cutaneous mastocytosis +
cutaneous porphyria
cutis laxa +
cysticercosis
dermatitis +
dermatomycosis +
dermatomyositis +
dioctophymiasis
dipetalonemiasis
dirofilariasis
eczema herpeticum
epidermal nevus
erythema multiforme
erythematosquamous dermatosis
erythrokeratodermia variabilis +
exanthem +
eyelid disease +
facial dermatosis
facioscapulohumeral muscular dystrophy 2
facioscapulohumeral muscular dystrophy 3
facioscapulohumeral muscular dystrophy 4
familial progressive hyperpigmentation with or without hypopigmentation
filarial elephantiasis
granulomatosis with polyangiitis
hand dermatosis
hemorrhoid +
hereditary coproporphyria
hereditary hypophosphatemic rickets with hypercalciuria
hypomelanosis of Ito
ichthyosis +
iminoglycinuria
inflammatory poikiloderma with hair abnormalities and acral keratoses
isolated hyperchlorhidrosis
Joubert syndrome 15
Joubert syndrome 9
keratosis +
Kimura disease
Kindler syndrome
large congenital melanocytic nevus
leg dermatosis
lichen disease +
lipomatosis +
loiasis
long QT syndrome 1
long QT syndrome 2
long QT syndrome 3
long QT syndrome 5
long QT syndrome 6
long QT syndrome 9
mansonelliasis
methylmalonic aciduria and homocystinuria type cblC
mongolian spot
multiple benign circumferential skin creases on limbs +
multiple cutaneous and mucosal venous malformations
necrobiosis lipoidica
Netherton syndrome
nonsyndromic aplasia cutis congenita
ocular albinism with sensorineural deafness
oculocutaneous albinism type IB
panniculitis +
Parkinson's disease 6
peeling skin syndrome +
pigmentation disease +
pityriasis rubra pilaris
PLACK syndrome
poikiloderma with neutropenia
primary cutaneous amyloidosis +
primary pulmonary hypertension
proteasome-associated autoinflammatory syndrome 1
proteasome-associated autoinflammatory syndrome 3
Pthirus pubis infestation
reactive cutaneous fibrous lesion +
restrictive dermopathy +
retinitis pigmentosa 7
Ritter's disease +
rosacea
Rothmund-Thomson syndrome
scalp dermatosis
scleredema adultorum
sebaceous gland disease +
short-rib thoracic dysplasia 7 with or without polydactyly
skin atrophy
skin benign neoplasm +
skin cancer +
skin carcinoma in situ
skin sarcoidosis
smallpox +
spinocerebellar ataxia type 17
Stevens-Johnson syndrome
stiff skin syndrome
strongyloidiasis
sweat gland disease +
Sweet syndrome
tinea barbae
tinea corporis +
tinea manuum
tinea pedis
tyrosinemia type II
urticaria +
Usher syndrome type 1D
Usher syndrome type 2C
UV-sensitive syndrome
vascular skin disease
verruciform xanthoma of skin
Waardenburg syndrome type 2A
white sponge nevus +
yellow nail syndrome

autosomal dominant dyskeratosis congenita 1
autosomal dominant dyskeratosis congenita 2
autosomal dominant dyskeratosis congenita 3
autosomal dominant dyskeratosis congenita 4
autosomal dominant dyskeratosis congenita 6
autosomal recessive dyskeratosis congenita 1
autosomal recessive dyskeratosis congenita 2
autosomal recessive dyskeratosis congenita 3
autosomal recessive dyskeratosis congenita 4
autosomal recessive dyskeratosis congenita 5
autosomal recessive dyskeratosis congenita 6
digenic dyskeratosis congenita
Revesz syndrome
X-linked dyskeratosis congenita