Thick vermilion border

Symptom Information:

Symptom ID: HPO:0012471
Synonyms:
Full lips [HPO:0012471]
Thick lips [HPO:0012471]
Full lips [OMIM:Full lips]
Thick lips [OMIM:Thick lips]
Lips full [OMIM:Lips full]
Thick lips (in males) [OMIM:Thick lips (in males)]
Quality:
Cross references:
OMIM: "Full lips" [OMIM:Full lips]
OMIM: "Thick lips" [OMIM:Thick lips]
OMIM: "Lips full" [OMIM:Lips full]
OMIM: "Thick lips (in males)" [OMIM:Thick lips (in males)]
Is a (Direct Parents):
HPO         Abnormality of the lip
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:
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)