Thick vermilion border
Symptom Information:
Symptom ID: | HPO:0012471 | ||||||
Synonyms: |
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Quality: | |||||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the mouth(HPO:0000153) Abnormality of the lip(HPO:0000159) Thick vermilion border(HPO:0012471) MedDRA: |
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Database Frequency: | 115 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
16q24.3 microdeletion syndrome | (Orphanet:261250) |
8p23.1 microduplication syndrome | (Orphanet:251076) |
Ackerman syndrome | (Orphanet:2561) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Acromegaly | (Orphanet:963) |
Acromicric dysplasia | (Orphanet:969) |
Alpha-N-acetylgalactosaminidase deficiency | (Orphanet:3137) |
Alpha-N-acetylgalactosaminidase deficiency type 2 | (Orphanet:79280) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis | (Orphanet:86818) |
Aspartylglucosaminuria | (Orphanet:93) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
Blackfan-Diamond anemia | (Orphanet:124) |
Blepharophimosis - ptosis - esotropia - syndactyly - short stature | (Orphanet:2057) |
CANDLE syndrome | (Orphanet:325004) |
CLARK-BARAITSER SYNDROME | (OMIM:300602) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
Cataract-congenital heart disease-neural tube defect syndrome | (Orphanet:314993) |
Char syndrome | (Orphanet:46627) |
Cheilitis glandularis | (Orphanet:1221) |
Coffin-Lowry syndrome | (Orphanet:192) |
Coffin-Siris syndrome | (Orphanet:1465) |
Costello syndrome | (Orphanet:3071) |
Craniofaciofrontodigital syndrome | (Orphanet:363705) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
Deafness - onychodystrophy | (Orphanet:3231) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Down syndrome | (Orphanet:870) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 | (OMIM:615859) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Encephalopathy due to sulfite oxidase deficiency | (Orphanet:833) |
Fabry disease | (Orphanet:324) |
Feingold syndrome | (Orphanet:1305) |
Fountain syndrome | (Orphanet:3219) |
Fryns-Smeets-Thiry syndrome | (Orphanet:2058) |
Fucosidosis | (Orphanet:349) |
Gingival fibromatosis - facial dysmorphism | (Orphanet:2025) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
Hypospadias - hypertelorism - coloboma and deafness | (Orphanet:157788) |
Intellectual deficit, Wolff type | (Orphanet:3080) |
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures | (Orphanet:1568) |
Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
Intellectual deficit, X-linked, Wilson type | (Orphanet:85290) |
Ito hypomelanosis | (Orphanet:435) |
JMP syndrome | (Orphanet:324999) |
KAHRIZI SYNDROME | (OMIM:612713) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
Leprechaunism | (Orphanet:508) |
Lipoid proteinosis | (Orphanet:530) |
MACS syndrome | (Orphanet:217335) |
MEHMO syndrome | (Orphanet:85282) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MEIER-GORLIN SYNDROME 3 | (OMIM:613803) |
MEIER-GORLIN SYNDROME 4 | (OMIM:613804) |
MEIER-GORLIN SYNDROME 5 | (OMIM:613805) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 | (OMIM:615866) |
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA | (OMIM:608624) |
MOMO syndrome | (Orphanet:2563) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
Marshall syndrome | (Orphanet:560) |
Melkersson-Rosenthal syndrome | (Orphanet:2483) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type | (Orphanet:217026) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 6 | (Orphanet:583) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Multiple endocrine neoplasia type 2B | (Orphanet:247709) |
NOONAN SYNDROME 4 | (OMIM:610733) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Neu-Laxova syndrome | (Orphanet:2671) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Odonto-tricho-ungual-digito-palmar syndrome | (Orphanet:69082) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Proteasome disability syndrome | (Orphanet:324977) |
Ptosis - upper ocular movement limitation - absence of lacrimal punctum | (Orphanet:228396) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Recombinant 8 syndrome | (Orphanet:96167) |
SLC35A2-CDG | (Orphanet:356961) |
SPONASTRIME dysplasia | (Orphanet:93357) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES | (OMIM:600093) |
Sanfilippo syndrome type D | (Orphanet:79272) |
Scheie syndrome | (Orphanet:93474) |
Sialidosis type 1 | (Orphanet:812) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Stoll-Alembik-Finck syndrome | (Orphanet:3200) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |
THREE M SYNDROME 1 | (OMIM:273750) |
THREE M SYNDROME 2 | (OMIM:612921) |
Temtamy syndrome | (Orphanet:1777) |
Torg-Winchester syndrome | (Orphanet:3460) |
Trisomy 17p | (Orphanet:261290) |
Williams syndrome | (Orphanet:904) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |
Zimmermann-Laband syndrome | (Orphanet:3473) |
Zunich-Kaye syndrome | (Orphanet:3474) |