Cavernous hemangioma
Symptom Information:
Symptom ID: | HPO:0001048 | ||||||||||||||||||||||||||||||||||||||||||||||
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) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Vascular neoplasm(HPO:0100742) Hemangioma(HPO:0001028) Cavernous hemangioma(HPO:0001048) 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) MedDRA: Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Vascular neoplasm(HPO:0100742) Cavernous hemangioma(HPO:0001048) |
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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) |