Hemangioma

Symptom Information:

Symptom ID: HPO:0001028
Synonyms:
Hemangiomata [HPO:0001028]
Hemangioma [OMIM:Hemangioma]
Hemangiomata [OMIM:Hemangiomata]
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:
OMIM: "Hemangioma" [OMIM:Hemangioma]
OMIM: "Hemangiomata" [OMIM:Hemangiomata]
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)]
Is a (Direct Parents):
HPO         Neoplasm of the skin
HPO         Vascular neoplasm
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)
             Neoplasm of the skin(HPO:0008069)
                Hemangioma(HPO:0001028)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Neoplasm of the skin(HPO:0008069)
                Hemangioma(HPO:0001028)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Vascular neoplasm(HPO:0100742)
                Hemangioma(HPO:0001028)
MedDRA:
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

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)
COFFIN-SIRIS SYNDROME (OMIM:135900)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Chuvash erythrocytosis (Orphanet:238557)
Coffin-Siris syndrome (Orphanet:1465)
Costello syndrome (Orphanet:3071)
DPM1-CDG (Orphanet:79322)
Enchondromatosis (Orphanet:296)
Galactosialidosis (Orphanet:351)
Hereditary neurocutaneous angioma (Orphanet:1062)
Kasabach-Merritt syndrome (Orphanet:2330)
LYMPHEDEMA, HEREDITARY, IA (OMIM:153100)
Linear nevus sebaceus syndrome (Orphanet:2612)
Milroy disease (Orphanet:79452)
Mulibrey nanism (Orphanet:2576)
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO (OMIM:171300)
Proteus syndrome (Orphanet:744)
Ulnar/fibula ray defect - brachydactyly (Orphanet:52056)
Wolf-Hirschhorn syndrome (Orphanet:280)