Parent term(s)
Term with siblings
dipetalonemiasis

Achenbach syndrome
adermatoglyphia
Aland Island eye disease
amblyopia +
ancylostomiasis
ancylostomiasis
angioedema +
angiostrongyliasis
anterior segment dysgenesis +
autoimmune disease of skin and connective tissue +
Axenfeld-Rieger syndrome +
baylisascariasis
Birt-Hogg-Dube syndrome
blindness +
Brooke-Spiegler syndrome
cellulitis +
cercarial dermatitis
chancroid
cherubism
chorioretinitis +
chronic mucocutaneous candidiasis
chronic ulcer of skin +
coenurosis
Cogan syndrome
Cogan-Reese syndrome
coloboma
conjunctival disease +
contagious pustular dermatitis
corneal disease +
cutaneous anthrax
cutaneous candidiasis
cutaneous leishmaniasis
cutaneous lupus erythematosus +
cutaneous mastocytosis +
cutaneous porphyria
cutis laxa +
cysticercosis
cysticercosis
dermatitis +
dermatomycosis +
dermatomyositis +
dioctophymiasis
dirofilariasis
dirofilariasis
dyskeratosis congenita +
ectopia lentis with ectopia of pupil
eczema herpeticum
epidermal nevus
erythema multiforme
erythematosquamous dermatosis
erythrokeratodermia variabilis +
exanthem +
eye accommodation disease +
eye carcinoma in situ
eye degenerative disease +
eyelid disease +
facial dermatosis
familial progressive hyperpigmentation with or without hypopigmentation
filarial elephantiasis
filarial elephantiasis
Finnish type amyloidosis
fundus dystrophy +
glaucoma +
globe disease +
granulomatosis with polyangiitis
hand dermatosis
hemorrhoid +
hypomelanosis of Ito
ichthyosis +
inflammatory poikiloderma with hair abnormalities and acral keratoses
isolated hyperchlorhidrosis
keratoconjunctivitis +
keratosis +
Kimura disease
Kindler syndrome
lacrimal apparatus disease +
large congenital melanocytic nevus
leg dermatosis
lens disease +
lichen disease +
lipomatosis +
loiasis
loiasis
loiasis
mansonelliasis
mansonelliasis
Marfan syndrome
microphthalmia +
mongolian spot
multiple benign circumferential skin creases on limbs +
multiple cutaneous and mucosal venous malformations
necrobiosis lipoidica
Netherton syndrome
neuroretinitis
nonsyndromic aplasia cutis congenita
ocular albinism 1 +
ocular cancer +
ocular hypertension
ocular hypotension +
ocular motility disease +
ocular motor apraxia, Cogan type
ocular tuberculosis
onchocerciasis
ophthalmia nodosa
ophthalmomyiasis
panniculitis +
peeling skin syndrome +
philophthalmiasis
pigment dispersion syndrome
pigmentation disease +
pigmented paravenous chorioretinal atrophy
pityriasis rubra pilaris
PLACK syndrome
poikiloderma with neutropenia
primary cutaneous amyloidosis +
ptosis +
pupil disease +
reactive cutaneous fibrous lesion +
refractive error +
restrictive dermopathy +
retinal disease +
Ritter's disease
rosacea
Rothmund-Thomson syndrome
scalp dermatosis
scleral disease +
scleredema adultorum
scotoma
sebaceous gland disease +
setariasis
skin atrophy
skin benign neoplasm +
skin cancer +
skin carcinoma in situ
skin sarcoidosis
smallpox +
Stevens-Johnson syndrome
stiff skin syndrome
strongyloidiasis
Sveinsson chorioretinal atrophy
sweat gland disease +
Sweet syndrome
tinea barbae
tinea corporis +
tinea manuum
tinea pedis
toxocariasis
trachoma
tyrosinemia type II
urticaria +
UV-sensitive syndrome
uveal disease +
vascular skin disease
verruciform xanthoma of skin
visual impairment and progressive phthisis bulbi
visual pathway disease +
vitreous disease +
white sponge nevus +
yellow nail syndrome
Child term(s)

is-a denotes an 'is-a' relationship