Nevus flammeus

Symptom Information:

Symptom ID: HPO:0001052
Synonyms:
port-wine stain [HPO:0001052]
Port-wine stain [Orphanet:23650]
Port-wine stain of skin (disorder) [Orphanet:23650]
Salmon patch nevus (disorder) [Orphanet:23650]
Port-Wine Stain [Orphanet:23650]
Nevus flammeus [OMIM:Nevus flammeus]
Port-wine stain [OMIM:Port-wine stain]
Capillary hemangioma/nevus/naevus flammeus/port-wine stain [Orphanet:23650]
Naevus flammeus [HPO:0001052]
Naevus flammeus [Orphanet:23650]
Naevus flammeus [MedDRA:10067193]
Port wine naevus [MedDRA:10067193]
Port wine stain [MedDRA:10067193]
Salmon patch [MedDRA:10067193]
Port wine nevus [MedDRA:10067193]
Nevus flammeus [MedDRA:10067193]
Stork bite [MedDRA:10067193]
Nevi flammei (philtrum, nape of neck, forehead) [OMIM:Nevi flammei (philtrum, nape of neck, forehead)]
Nevus flammeus (eyelids and nape of neck) [OMIM:Nevus flammeus (eyelids and nape of neck)]
Nevus flammeus (eyelids) [OMIM:Nevus flammeus (eyelids)]
Quality:
Cross references:
Orphanet:23650 "Capillary hemangioma/nevus/naevus flammeus/port-wine stain" [Orphanet:23650]
OMIM: "Nevus flammeus" [OMIM:Nevus flammeus]
OMIM: "Port-wine stain" [OMIM:Port-wine stain]
OMIM: "Nevi flammei (philtrum, nape of neck, forehead)" [OMIM:Nevi flammei (philtrum, nape of neck, forehead)]
OMIM: "Nevus flammeus (eyelids and nape of neck)" [OMIM:Nevus flammeus (eyelids and nape of neck)]
OMIM: "Nevus flammeus (eyelids)" [OMIM:Nevus flammeus (eyelids)]
UMLS:C0235752 "Port-Wine Stain" [Orphanet:23650]
Is a (Direct Parents):
MedDRA Vascular malformations and acquired anomalies
HPO         Arteriovenous malformation
Orphanet Vascular skin abnormality
HPO         Nevus
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)