Parent term(s)
physical disorder
+
skin disease
+
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)
denotes an 'is-a' relationship