Cavernous hemangioma

Symptom Information:

Symptom ID: HPO:0001048
Synonyms:
Cavernous haemangioma [HPO:0001048]
Cavernous angioma [Orphanet:23660]
Cavernous hemangioma (morphologic abnormality) [Orphanet:23660]
Cavernous hemangioma (disorder) [Orphanet:23660]
Hemangioma, Cavernous [Orphanet:23660]
Angioma, Cavernous [Orphanet:23660]
Cavernous hemangioma [OMIM:Cavernous hemangioma]
Cavernous/tuberous hemangioma [Orphanet:23660]
Haemangioma cavernous [HPO:0001048]
Haemangioma cavernous [Orphanet:23660]
Haemangioma [MedDRA:10018814]
Acquired haemangioma [MedDRA:10018814]
Acquired hemangioma [MedDRA:10018814]
Angioma [MedDRA:10018814]
Angioma (benign) [MedDRA:10018814]
Haemangioma acquired [MedDRA:10018814]
Haemangioma and lymphangioma, any site [MedDRA:10018814]
Haemangioma aquired [MedDRA:10018814]
Haemangioma NOS [MedDRA:10018814]
Haemangioma, any site [MedDRA:10018814]
Hemangioma [MedDRA:10018814]
Hemangioma acquired [MedDRA:10018814]
Hemangioma and lymphangioma, any site [MedDRA:10018814]
Hemangioma arterial [MedDRA:10018814]
Hemangioma cavernous [MedDRA:10018814]
Hemangioma extensum [MedDRA:10018814]
Hemangioma NOS [MedDRA:10018814]
Hemangioma of other sites [MedDRA:10018814]
Hemangioma of unspecified site [MedDRA:10018814]
Hemangioma sclerosing [MedDRA:10018814]
Hemangioma senile [MedDRA:10018814]
Hemangioma, any site [MedDRA:10018814]
Nevus vascular [MedDRA:10018814]
Haemangioma arterial [MedDRA:10018814]
Haemangioma cavernous [MedDRA:10018814]
Haemangioma extensum [MedDRA:10018814]
Haemangioma of unspecified site [MedDRA:10018814]
Haemangioma sclerosing [MedDRA:10018814]
Haemangioma senile [MedDRA:10018814]
Naevus vascular [MedDRA:10018814]
Cavernoma [MedDRA:10018814]
Angiomas [OMIM:Angiomas]
Hemangioma (neck and forehead) [OMIM:Hemangioma (neck and forehead)]
Hemangiomas [OMIM:Hemangiomas]
Hemangiomas (facial, glabellar) [OMIM:Hemangiomas (facial, glabellar)]
Hemangiomata (Maffucci type) [OMIM:Hemangiomata (Maffucci type)]
Quality:
Cross references:
Orphanet:23660 "Cavernous/tuberous hemangioma" [Orphanet:23660]
OMIM: "Cavernous hemangioma" [OMIM:Cavernous hemangioma]
OMIM: "Angiomas" [OMIM:Angiomas]
OMIM: "Hemangioma (neck and forehead)" [OMIM:Hemangioma (neck and forehead)]
OMIM: "Hemangiomas" [OMIM:Hemangiomas]
OMIM: "Hemangiomas (facial, glabellar)" [OMIM:Hemangiomas (facial, glabellar)]
OMIM: "Hemangiomata (Maffucci type)" [OMIM:Hemangiomata (Maffucci type)]
UMLS:C0018920 "Hemangioma, Cavernous" [Orphanet:23660]
UMLS:C1959589 "Angioma, Cavernous" [Orphanet:23660]
Is a (Direct Parents):
MedDRA Vascular neoplasm
Orphanet Vascular skin abnormality
HPO         Hemangioma
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Vascular neoplasm(HPO:0100742)
                Hemangioma(HPO:0001028)
                   Cavernous hemangioma(HPO:0001048)
             Neoplasm of the skin(HPO:0008069)
                Hemangioma(HPO:0001028)
                   Cavernous hemangioma(HPO:0001048)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Neoplasm of the skin(HPO:0008069)
                Hemangioma(HPO:0001028)
                   Cavernous hemangioma(HPO:0001048)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Vascular neoplasm(HPO:0100742)
                Hemangioma(HPO:0001028)
                   Cavernous hemangioma(HPO:0001048)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular neoplasm(HPO:0100742)
          Cavernous hemangioma(HPO:0001048)
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

ADAMS-OLIVER SYNDROME 5 (OMIM:616028)
Aicardi syndrome (Orphanet:50)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Autosomal recessive omodysplasia (Orphanet:93329)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Blue rubber bleb nevus (Orphanet:1059)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cataract - aberrant oral frenula - growth delay (Orphanet:1373)
Cavernous hemangiomas of face - supraumbilical midline raphe (Orphanet:2124)
Cowden syndrome (Orphanet:201)
DE SANCTIS-CACCHIONE SYNDROME (OMIM:278800)
DPM1-CDG (Orphanet:79322)
Dandy-Walker malformation - facial hemangioma (Orphanet:1564)
Enchondromatosis (Orphanet:296)
HEMANGIOMAS OF SMALL INTESTINE (OMIM:140900)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Linear nevus sebaceus syndrome (Orphanet:2612)
Mucolipidosis type 2 (Orphanet:576)
Sternal malformation - vascular dysplasia (Orphanet:3195)
Transverse limb deficiency - hemangioma (Orphanet:2486)
Ulnar/fibula ray defect - brachydactyly (Orphanet:52056)
VACTERL/VATER association (Orphanet:887)
X-linked centronuclear myopathy (Orphanet:596)
Xeroderma pigmentosum complementation group A (Orphanet:276249)
Xeroderma pigmentosum complementation group D (Orphanet:276258)
Xeroderma pigmentosum complementation group E (Orphanet:276261)
Xeroderma pigmentosum variant (Orphanet:90342)