Parent term(s)
Term with siblings
Achenbach syndrome
adermatoglyphia
Alport syndrome +
ancylostomiasis
angioedema +
anterior segment dysgenesis +
autoimmune disease of skin and connective tissue +
autosomal genetic disease +
Bartter disease +
basal laminar drusen
Birt-Hogg-Dube syndrome
Brooke-Spiegler syndrome
Brugada syndrome +
Camurati-Engelmann disease
cardiofaciocutaneous syndrome +
cataract +
catecholaminergic polymorphic ventricular tachycardia +
cellulitis +
cercarial dermatitis
chancroid
cherubism
chondrodysplasia punctata +
chronic mucocutaneous candidiasis
chronic ulcer of skin +
ciliopathy +
coenurosis
cone-rod dystrophy +
contagious pustular dermatitis
contractures, pterygia, and spondylocarpotarsal fusion syndrome +
Cornelia de Lange syndrome +
corticosteroid-binding globulin deficiency
cutaneous anthrax
cutaneous candidiasis
cutaneous leishmaniasis
cutaneous lupus erythematosus +
cutaneous mastocytosis +
cutaneous porphyria
cutis laxa +
cysticercosis
dermatitis +
dermatomycosis +
dermatomyositis +
dilated cardiomyopathy 1BB
dilated cardiomyopathy 1EE
dilated cardiomyopathy 1FF
dilated cardiomyopathy 1G
dilated cardiomyopathy 1GG
dilated cardiomyopathy 1H
dilated cardiomyopathy 1I
dilated cardiomyopathy 1J
dilated cardiomyopathy 1K
dilated cardiomyopathy 1L
dilated cardiomyopathy 1M
dilated cardiomyopathy 1O
dilated cardiomyopathy 1P
dilated cardiomyopathy 1Q
dilated cardiomyopathy 1T
dilated cardiomyopathy 1W
dilated cardiomyopathy 1Z
dioctophymiasis
dipetalonemiasis
dirofilariasis
dyskeratosis congenita +
eczema herpeticum
epidermal nevus
erythema multiforme
erythematosquamous dermatosis
exanthem +
eyelid disease +
facial dermatosis
familial hemophagocytic lymphohistiocytosis 5
familial nephrotic syndrome +
familial progressive hyperpigmentation with or without hypopigmentation
Fanconi anemia complementation group F
Fanconi anemia complementation group G
Fanconi anemia complementation group J
Fanconi anemia complementation group N
fetal akinesia deformation sequence syndrome +
filarial elephantiasis
gene duplication disease +
granulomatosis with polyangiitis
hand dermatosis
hemorrhoid +
hereditary combined deficiency of vitamin K-dependent clotting factors +
hypochondrogenesis
hypomelanosis of Ito
ichthyosis +
infantile histiocytoid cardiomyopathy
inflammatory bowel disease 1
inflammatory bowel disease 10
inflammatory bowel disease 11
inflammatory bowel disease 12
inflammatory bowel disease 13
inflammatory bowel disease 14
inflammatory bowel disease 15
inflammatory bowel disease 16
inflammatory bowel disease 17
inflammatory bowel disease 18
inflammatory bowel disease 19
inflammatory bowel disease 2
inflammatory bowel disease 20
inflammatory bowel disease 22
inflammatory bowel disease 23
inflammatory bowel disease 24
inflammatory bowel disease 26
inflammatory bowel disease 27
inflammatory bowel disease 4
inflammatory bowel disease 5
inflammatory bowel disease 6
inflammatory bowel disease 7
inflammatory bowel disease 8
inflammatory bowel disease 9
inflammatory poikiloderma with hair abnormalities and acral keratoses
isolated hyperchlorhidrosis
isolated microphthalmia 4
keratosis +
Kimura disease
Kindler syndrome
lambda 5 deficiency
large congenital melanocytic nevus
Leber congenital amaurosis 10
Leber congenital amaurosis 3
Leber congenital amaurosis 7
leg dermatosis
lichen disease +
lipomatosis +
loiasis
mansonelliasis
mongolian spot
multiple benign circumferential skin creases on limbs +
multiple cutaneous and mucosal venous malformations
multiple epiphyseal dysplasia due to collagen 9 anomaly +
necrobiosis lipoidica
Netherton syndrome
nonsyndromic aplasia cutis congenita
Noonan syndrome +
osteogenesis imperfecta type 14
osteogenesis imperfecta type 6
panniculitis +
peeling skin syndrome +
pigmentation disease +
pityriasis rubra pilaris
PLACK syndrome
poikiloderma with neutropenia
posterior polymorphous corneal dystrophy 3
postural orthostatic tachycardia syndrome
primary congenital glaucoma +
primary cutaneous amyloidosis +
reactive cutaneous fibrous lesion +
restrictive dermopathy +
Ritscher-Schinzel syndrome +
Ritter's disease
rosacea
Rothmund-Thomson syndrome
scalp dermatosis
schizophrenia 13
schizophrenia 14
schizophrenia 16
schizophrenia 18
schizophrenia 9
scleredema adultorum
sebaceous gland disease +
SHOX-related short stature
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
tyrosinemia type II
urticaria +
UV-sensitive syndrome
vascular skin disease
verruciform xanthoma of skin
white sponge nevus +
X-linked monogenic disease +
Y-linked monogenic disease +
yellow nail syndrome
erythrokeratodermia variabilis +
Achenbach syndrome
adermatoglyphia
Alport syndrome +
ancylostomiasis
angioedema +
anterior segment dysgenesis +
autoimmune disease of skin and connective tissue +
autosomal genetic disease +
Bartter disease +
basal laminar drusen
Birt-Hogg-Dube syndrome
Brooke-Spiegler syndrome
Brugada syndrome +
Camurati-Engelmann disease
cardiofaciocutaneous syndrome +
cataract +
catecholaminergic polymorphic ventricular tachycardia +
cellulitis +
cercarial dermatitis
chancroid
cherubism
chondrodysplasia punctata +
chronic mucocutaneous candidiasis
chronic ulcer of skin +
ciliopathy +
coenurosis
cone-rod dystrophy +
contagious pustular dermatitis
contractures, pterygia, and spondylocarpotarsal fusion syndrome +
Cornelia de Lange syndrome +
corticosteroid-binding globulin deficiency
cutaneous anthrax
cutaneous candidiasis
cutaneous leishmaniasis
cutaneous lupus erythematosus +
cutaneous mastocytosis +
cutaneous porphyria
cutis laxa +
cysticercosis
dermatitis +
dermatomycosis +
dermatomyositis +
dilated cardiomyopathy 1BB
dilated cardiomyopathy 1EE
dilated cardiomyopathy 1FF
dilated cardiomyopathy 1G
dilated cardiomyopathy 1GG
dilated cardiomyopathy 1H
dilated cardiomyopathy 1I
dilated cardiomyopathy 1J
dilated cardiomyopathy 1K
dilated cardiomyopathy 1L
dilated cardiomyopathy 1M
dilated cardiomyopathy 1O
dilated cardiomyopathy 1P
dilated cardiomyopathy 1Q
dilated cardiomyopathy 1T
dilated cardiomyopathy 1W
dilated cardiomyopathy 1Z
dioctophymiasis
dipetalonemiasis
dirofilariasis
dyskeratosis congenita +
eczema herpeticum
epidermal nevus
erythema multiforme
erythematosquamous dermatosis
exanthem +
eyelid disease +
facial dermatosis
familial hemophagocytic lymphohistiocytosis 5
familial nephrotic syndrome +
familial progressive hyperpigmentation with or without hypopigmentation
Fanconi anemia complementation group F
Fanconi anemia complementation group G
Fanconi anemia complementation group J
Fanconi anemia complementation group N
fetal akinesia deformation sequence syndrome +
filarial elephantiasis
gene duplication disease +
granulomatosis with polyangiitis
hand dermatosis
hemorrhoid +
hereditary combined deficiency of vitamin K-dependent clotting factors +
hypochondrogenesis
hypomelanosis of Ito
ichthyosis +
infantile histiocytoid cardiomyopathy
inflammatory bowel disease 1
inflammatory bowel disease 10
inflammatory bowel disease 11
inflammatory bowel disease 12
inflammatory bowel disease 13
inflammatory bowel disease 14
inflammatory bowel disease 15
inflammatory bowel disease 16
inflammatory bowel disease 17
inflammatory bowel disease 18
inflammatory bowel disease 19
inflammatory bowel disease 2
inflammatory bowel disease 20
inflammatory bowel disease 22
inflammatory bowel disease 23
inflammatory bowel disease 24
inflammatory bowel disease 26
inflammatory bowel disease 27
inflammatory bowel disease 4
inflammatory bowel disease 5
inflammatory bowel disease 6
inflammatory bowel disease 7
inflammatory bowel disease 8
inflammatory bowel disease 9
inflammatory poikiloderma with hair abnormalities and acral keratoses
isolated hyperchlorhidrosis
isolated microphthalmia 4
keratosis +
Kimura disease
Kindler syndrome
lambda 5 deficiency
large congenital melanocytic nevus
Leber congenital amaurosis 10
Leber congenital amaurosis 3
Leber congenital amaurosis 7
leg dermatosis
lichen disease +
lipomatosis +
loiasis
mansonelliasis
mongolian spot
multiple benign circumferential skin creases on limbs +
multiple cutaneous and mucosal venous malformations
multiple epiphyseal dysplasia due to collagen 9 anomaly +
necrobiosis lipoidica
Netherton syndrome
nonsyndromic aplasia cutis congenita
Noonan syndrome +
osteogenesis imperfecta type 14
osteogenesis imperfecta type 6
panniculitis +
peeling skin syndrome +
pigmentation disease +
pityriasis rubra pilaris
PLACK syndrome
poikiloderma with neutropenia
posterior polymorphous corneal dystrophy 3
postural orthostatic tachycardia syndrome
primary congenital glaucoma +
primary cutaneous amyloidosis +
reactive cutaneous fibrous lesion +
restrictive dermopathy +
Ritscher-Schinzel syndrome +
Ritter's disease
rosacea
Rothmund-Thomson syndrome
scalp dermatosis
schizophrenia 13
schizophrenia 14
schizophrenia 16
schizophrenia 18
schizophrenia 9
scleredema adultorum
sebaceous gland disease +
SHOX-related short stature
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
tyrosinemia type II
urticaria +
UV-sensitive syndrome
vascular skin disease
verruciform xanthoma of skin
white sponge nevus +
X-linked monogenic disease +
Y-linked monogenic disease +
yellow nail syndrome
Child term(s)
denotes an 'is-a' relationship