Capillary hemangiomas
Symptom Information:
Symptom ID: | HPO:0005306 | |||||||||||||||||||||||||||||||||||||||||
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 integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Neoplasm of the skin(HPO:0008069) Hemangioma(HPO:0001028) Capillary hemangiomas(HPO:0005306) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the skin(HPO:0008069) Hemangioma(HPO:0001028) Capillary hemangiomas(HPO:0005306) Vascular neoplasm(HPO:0100742) Hemangioma(HPO:0001028) Capillary hemangiomas(HPO:0005306) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Vascular neoplasm(HPO:0100742) Hemangioma(HPO:0001028) Capillary hemangiomas(HPO:0005306) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Skin and subcutaneous tissue disorders congenital(MedDRA:10040789) Skin and subcutaneous tissue disorders congenital NEC(MedDRA:10040834) Capillary hemangiomas(HPO:0005306) Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Vascular malformations and acquired anomalies(MedDRA:10047091) Capillary hemangiomas(HPO:0005306) Vascular neoplasm(HPO:0100742) Capillary hemangiomas(HPO:0005306) |
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Database Frequency: | 8 / 7739 | |||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Capillary malformation - arteriovenous malformation | (Orphanet:137667) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
FRONTOOCULAR SYNDROME | (OMIM:605321) |
Familial capillary hemangioma | (Orphanet:91415) |
KAHRIZI SYNDROME | (OMIM:612713) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |