Nevus flammeus
Symptom Information:
Symptom ID: | HPO:0001052 | ||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||
Quality: | |||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Localized skin lesion(HPO:0011355) Nevus(HPO:0003764) Nevus flammeus(HPO:0001052) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Arteriovenous malformation(HPO:0100026) Nevus flammeus(HPO:0001052) MedDRA: Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Vascular malformations and acquired anomalies(MedDRA:10047091) Nevus flammeus(HPO:0001052) |
||||||||||||||||||||
Database Frequency: | 88 / 7739 | ||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3C syndrome | (Orphanet:7) |
Acrocephalosyndactyly | (Orphanet:946) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
Angioma serpiginosum | (Orphanet:95429) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Autosomal recessive omodysplasia | (Orphanet:93329) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Beckwith-Wiedemann syndrome due to 11p15 microduplication | (Orphanet:96076) |
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion | (Orphanet:231130) |
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Bone dysplasia, lethal Holmgren type | (Orphanet:1842) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
C syndrome | (Orphanet:1308) |
CLAPO syndrome | (Orphanet:168984) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Castleman disease | (Orphanet:160) |
Cobb syndrome | (Orphanet:53721) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
Diffuse neonatal hemangiomatosis | (Orphanet:2123) |
Dyschromatosis universalis | (Orphanet:241) |
Dysspondyloenchondromatosis | (Orphanet:85198) |
EEC syndrome | (Orphanet:1896) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
FRONTOOCULAR SYNDROME | (OMIM:605321) |
Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
Familial melanoma | (Orphanet:618) |
Familial multiple nevi flammei | (Orphanet:624) |
GAPO syndrome | (Orphanet:2067) |
Hereditary neurocutaneous angioma | (Orphanet:1062) |
Humero-radio-ulnar synostosis | (Orphanet:3266) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
Ito hypomelanosis | (Orphanet:435) |
Juvenile polyposis syndrome | (Orphanet:2929) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
Large congenital melanocytic nevus | (Orphanet:626) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
Maffucci syndrome | (Orphanet:163634) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Melorheostosis | (Orphanet:2485) |
Melorheostosis with osteopoikilosis | (Orphanet:1879) |
Mulibrey nanism | (Orphanet:2576) |
Nevus comedonicus syndrome | (Orphanet:64754) |
Non-distal trisomy 13q | (Orphanet:1702) |
Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
PELVIS syndrome | (Orphanet:83628) |
PHACE syndrome | (Orphanet:42775) |
Parkes Weber syndrome | (Orphanet:90307) |
Perlman syndrome | (Orphanet:2849) |
Phakomatosis pigmentovascularis | (Orphanet:2875) |
Port-wine nevi - mega cisterna magna - hydrocephalus | (Orphanet:2703) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Progressive osseous heteroplasia | (Orphanet:2762) |
Proteus syndrome | (Orphanet:744) |
Proteus-like syndrome | (Orphanet:2969) |
Pulmonary arterial hypertension | (Orphanet:182090) |
Radial ray hypoplasia - choanal atresia | (Orphanet:3026) |
Roberts syndrome | (Orphanet:3103) |
Rubinstein-Taybi syndrome | (Orphanet:783) |
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus | (Orphanet:137608) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
Sternal malformation - vascular dysplasia | (Orphanet:3195) |
Sturge-Weber syndrome | (Orphanet:3205) |
Syringocystadenoma papilliferum | (Orphanet:840) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Triopia | (Orphanet:3374) |
Trisomy 13 | (Orphanet:3378) |
Tuberous sclerosis | (Orphanet:805) |
Ulnar/fibula ray defect - brachydactyly | (Orphanet:52056) |
Von Hippel anomaly | (Orphanet:98941) |
Von Hippel-Lindau disease | (Orphanet:892) |
Williams syndrome | (Orphanet:904) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
Woolly hair - hypotrichosis - everted lower lip - outstanding ears | (Orphanet:1409) |
Wyburn-Mason syndrome | (Orphanet:53719) |
Xeroderma pigmentosum | (Orphanet:910) |