Visceral angiomatosis

Symptom Information:

Symptom ID: HPO:0100761
Synonyms:
Visceral angiomatosis (excluding skin) [Orphanet:34760]
Quality:
Cross references:
Orphanet:34760 "Visceral angiomatosis (excluding skin)" [Orphanet:34760]
Is a (Direct Parents):
HPO         Hemangiomatosis
Orphanet Structural anomalies of the cardio-circulatory system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the skin(HPO:0008069)
                Hemangioma(HPO:0001028)
                   Hemangiomatosis(HPO:0007461)
                      Visceral angiomatosis(HPO:0100761)
             Vascular neoplasm(HPO:0100742)
                Hemangioma(HPO:0001028)
                   Hemangiomatosis(HPO:0007461)
                      Visceral angiomatosis(HPO:0100761)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Vascular neoplasm(HPO:0100742)
                Hemangioma(HPO:0001028)
                   Hemangiomatosis(HPO:0007461)
                      Visceral angiomatosis(HPO:0100761)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Neoplasm of the skin(HPO:0008069)
                Hemangioma(HPO:0001028)
                   Hemangiomatosis(HPO:0007461)
                      Visceral angiomatosis(HPO:0100761)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Angio-osteohypertrophic syndrome (Orphanet:2346)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Blue rubber bleb nevus (Orphanet:1059)
Cerebral arteriovenous malformation (Orphanet:46724)
Cobb syndrome (Orphanet:53721)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Diastrophic dwarfism (Orphanet:628)
Diffuse neonatal hemangiomatosis (Orphanet:2123)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Enchondromatosis (Orphanet:296)
Fetal alcohol syndrome (Orphanet:1915)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Osteogenesis imperfecta (Orphanet:666)
PHACE syndrome (Orphanet:42775)
Proteus syndrome (Orphanet:744)
Secondary polycythemia (Orphanet:98428)
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus (Orphanet:137608)
Sternal malformation - vascular dysplasia (Orphanet:3195)
Tuberous sclerosis (Orphanet:805)
Von Hippel-Lindau disease (Orphanet:892)