Parent term(s)
Term with siblings
large congenital melanocytic nevus

Achenbach syndrome
adermatoglyphia
agnathia-otocephaly complex
ancylostomiasis
angioedema +
arthrogryposis multiplex congenita +
autoimmune disease of skin and connective tissue +
autosomal dominant congenital deafness with onychodystrophy
autosomal recessive congenital ichthyosis +
Birt-Hogg-Dube syndrome
bladder exstrophy-epispadias-cloacal exstrophy complex +
blepharophimosis
Brooke-Spiegler syndrome
caudal regression syndrome
cellulitis +
cercarial dermatitis
chancroid
cherubism
chronic mucocutaneous candidiasis
chronic ulcer of skin +
cleft palate-lateral synechia syndrome
coenurosis
Compton-North congenital myopathy
congenital adrenal hyperplasia
congenital adrenal insufficiency
congenital afibrinogenemia
congenital amegakaryocytic thrombocytopenia
congenital aphakia
congenital bilateral absence of vas deferens +
congenital bile acid synthesis defect +
congenital central hypoventilation syndrome
congenital chylothorax
congenital contractural arachnodactyly
congenital diaphragmatic hernia
congenital diarrhea +
congenital disorder of glycosylation +
congenital epulis
congenital fibrosarcoma
congenital fibrosis of the extraocular muscles +
congenital generalized lipodystrophy +
congenital granular cell tumor
congenital heart block
congenital heart defects, hamartomas of tongue, and polysyndactyly
congenital heart disease +
congenital hemolytic anemia +
congenital hereditary endothelial dystrophy of cornea
congenital hypogammaglobulinemia
congenital hypoplastic anemia +
congenital hypothyroidism +
congenital hypotrichosis with juvenile macular dystrophy
congenital intrinsic factor deficiency
congenital lactase deficiency
congenital leptin deficiency
congenital megabladder
congenital mesoblastic nephroma +
congenital mirror movement disorder
congenital muscular dystrophy +
congenital myasthenic syndrome +
congenital myopathy 4A +
congenital nervous system abnormality +
congenital nystagmus +
congenital ptosis
congenital secretory chloride diarrhea 1
congenital secretory sodium diarrhea 3
congenital secretory sodium diarrhea 8
congenital stationary night blindness +
congenital stromal corneal dystrophy
congenital structural myopathy +
congenital sucrase-isomaltase deficiency
congenital syphilis +
congenital toxoplasmosis
congenital vertical talus
contagious pustular dermatitis
contractures, pterygia, and spondylocarpotarsal fusion syndrome +
cryptophthalmia +
cutaneous anthrax
cutaneous candidiasis
cutaneous leishmaniasis
cutaneous lupus erythematosus +
cutaneous mastocytosis +
cutaneous porphyria
cutis laxa +
cysticercosis
dermatitis +
dermatomycosis +
dermatomyositis +
developmental cardiac valvular defect
dioctophymiasis
dipetalonemiasis
dirofilariasis
dyskeratosis congenita +
eczema herpeticum
epidermal nevus
epidermolysis bullosa with congenital localized absence of skin and deformity of nails
erythema multiforme
erythematosquamous dermatosis
erythrokeratodermia variabilis +
exanthem +
eyelid disease +
facial dermatosis
familial progressive hyperpigmentation with or without hypopigmentation
filarial elephantiasis
gastroschisis
granulomatosis with polyangiitis
hand dermatosis
hemorrhoid +
hypomelanosis of Ito
hypospadias
ichthyosis +
imperforate anus
inflammatory poikiloderma with hair abnormalities and acral keratoses
isolated hyperchlorhidrosis
keratosis +
Kimura disease
Kindler syndrome
Klippel-Feil syndrome +
laryngomalacia
Leber congenital amaurosis +
leg dermatosis
lethal congenital contracture syndrome +
lethal congenital glycogen storage disease of heart
lichen disease +
linear skin defects with multiple congenital anomalies 1
linear skin defects with multiple congenital anomalies 2
linear skin defects with multiple congenital anomalies 3
lipomatosis +
loiasis
mansonelliasis
Meckel's diverticulum
mongolian spot
multiple benign circumferential skin creases on limbs +
multiple congenital anomalies-hypotonia-seizures syndrome +
multiple cutaneous and mucosal venous malformations
myotonia congenita +
necrobiosis lipoidica
neonatal diabetes mellitus with congenital hypothyroidism
Netherton syndrome
neural tube defect +
non-congenital cyst of kidney
nonsyndromic aplasia cutis congenita
nonsyndromic congenital nail disorder +
omphalocele
orofacial cleft +
palmoplantar keratoderma and congenital alopecia 1
palmoplantar keratoderma and congenital alopecia 2
pancreatic hypoplasia-diabetes-congenital heart disease syndrome
panniculitis +
peeling skin syndrome +
pigmentation disease +
pityriasis rubra pilaris
PLACK syndrome
poikiloderma with neutropenia
Poland syndrome
polydactyly +
primary congenital glaucoma +
primary cutaneous amyloidosis +
Pthirus pubis infestation
radioulnar synostosis
rapidly involuting congenital hemangioma
reactive cutaneous fibrous lesion +
renal-hepatic-pancreatic dysplasia
restrictive dermopathy +
Ritter's disease +
rosacea
Rothmund-Thomson syndrome
scalp dermatosis
scleredema adultorum
sebaceous gland disease +
severe congenital encephalopathy due to MECP2 mutation
severe congenital neutropenia +
Silver-Russell syndrome
skin atrophy
skin benign neoplasm +
skin cancer +
skin carcinoma in situ
skin sarcoidosis
smallpox +
spondyloepiphyseal dysplasia with congenital joint dislocations
Stevens-Johnson syndrome
stiff skin syndrome
strongyloidiasis
sweat gland disease +
Sweet syndrome
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
tinea barbae
tinea corporis +
tinea manuum
tinea pedis
TORCH syndrome
tyrosinemia type II
urticaria +
UV-sensitive syndrome
vascular skin disease
verruciform xanthoma of skin
visceral heterotaxy +
white sponge nevus +
yellow nail syndrome
Zika virus congenital syndrome
Child term(s)

is-a denotes an 'is-a' relationship