Hemangioma
Symptom Information:
Symptom ID: | HPO:0001028 | |||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |