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Ontology Browser
Term:
rapidly involuting congenital hemangioma (DOID:0080895)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
hemangioma +     
physical disorder +     
acquired hemangioma 
agnathia-otocephaly complex  
arteriovenous malformation +   
arthrogryposis multiplex congenita +   
autosomal dominant congenital deafness with onychodystrophy  
autosomal recessive congenital ichthyosis +   
Bannayan-Riley-Ruvalcaba syndrome  
bladder exstrophy-epispadias-cloacal exstrophy complex +   
blepharophimosis +   
breast hemangioma +  
capillary hemangioma +   
caudal regression syndrome  
cavernous hemangioma +   
central nervous system hemangioma +   
Central Nervous System Venous Angioma  
cleft palate-lateral synechia syndrome  
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 Foot Deformities +   
congenital generalized lipodystrophy +   
congenital granular cell tumor 
congenital heart block +   
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 stationary night blindness +   
congenital stromal corneal dystrophy  
congenital structural myopathy +   
congenital sucrase-isomaltase deficiency  
congenital syphilis +  
congenital toxoplasmosis  
cryptophthalmia +   
Cutaneous Hemangiomatosis with Associated Features 
deep angioma +  
Disseminated Hemangiomatosis 
epidermolysis bullosa with congenital localized absence of skin and deformity of nails  
gastroschisis +   
glomeruloid hemangioma 
hemangioblastoma +   
Hemangioendothelioma +   
hemangioma of intra-abdominal structure +   
hemangioma of lung +  
hemangioma of orbit 
hemangioma of peripheral nerve 
Hemangiomas of Small Intestine 
Hereditary Neurocutaneous Angioma 
histiocytoid hemangioma +  
hobnail hemangioma 
hypospadias +   
imperforate anus +   
intracranial structure hemangioma +  
Kasabach-Merritt Syndrome +   
Klippel-Feil syndrome +   
large congenital melanocytic nevus  
laryngomalacia +   
Leber congenital amaurosis +   
lethal congenital contracture syndrome +   
lethal congenital glycogen storage disease of heart  
Littoral Cell Angioma of the Spleen 
Meckel's diverticulum 
MLS syndrome +   
multiple congenital anomalies-hypotonia-seizures syndrome +   
myotonia congenita +   
neural tube defect +   
non-congenital cyst of kidney 
nonsyndromic congenital nail disorder +   
omphalocele  
orofacial cleft +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Pascual Castroviejo Syndrome 
Poland syndrome 
polydactyly +   
primary congenital glaucoma +   
radioulnar synostosis +   
rapidly involuting congenital hemangioma 
A hemangioma that is characterized by complete regression. (DO)
sclerosing hemangioma +  
severe congenital encephalopathy due to MECP2 mutation  
severe congenital neutropenia +   
Silver-Russell syndrome +   
skin hemangioma +   
Spinal Arterial Venous Malformations with Cutaneous Hemangiomas 
spindle cell hemangioma 
spondyloepiphyseal dysplasia with congenital joint dislocations  
Sturge-Weber syndrome +   
subglottic angioma 
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
TORCH syndrome 
Tufted Angioma  
venous hemangioma 
visceral heterotaxy +   
Zika virus congenital syndrome 

Synonyms
Xrefs: NCI:C172207 ;   ORDO:141184
Definition Sources: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786408/ "DO" "DO"

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