Thin vermilion border

Symptom Information:

Symptom ID: HPO:0000233
Synonyms:
Thin lips [HPO:0000233]
THIN VERMILION BORDERS [HPO:0000233]
Thin vermillion [HPO:0000233]
Thin upper lip vermillon [Orphanet:9160]
Thin lips [OMIM:Thin lips]
Thin vermilion border [OMIM:Thin vermilion border]
Thin vermilion borders [OMIM:Thin vermilion borders]
Thin vermillion [OMIM:Thin vermillion]
Thin/retracted lips [Orphanet:9160]
Lips thin [OMIM:Lips thin]
Thin lips (in some patients) [OMIM:Thin lips (in some patients)]
Quality:
Cross references:
HPO:0000219 "Thin upper lip vermilion" [Orphanet:9160]
Orphanet:9160 "Thin/retracted lips" [Orphanet:9160]
OMIM: "Thin lips" [OMIM:Thin lips]
OMIM: "Thin vermilion border" [OMIM:Thin vermilion border]
OMIM: "Thin vermilion borders" [OMIM:Thin vermilion borders]
OMIM: "Thin vermillion" [OMIM:Thin vermillion]
OMIM: "Lips thin" [OMIM:Lips thin]
OMIM: "Thin lips (in some patients)" [OMIM:Thin lips (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the lip
Orphanet Thin upper lip vermilion
Orphanet Abnormality of the mouth
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)
                      Thin vermilion border(HPO:0000233)
MedDRA:
Database Frequency: 124 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
15q24 microdeletion syndrome (Orphanet:94065)
16p13.11 microdeletion syndrome (Orphanet:261236)
17q11.2 microduplication syndrome (Orphanet:139474)
19p13.12 microdeletion syndrome (Orphanet:254346)
19q13.11 microdeletion syndrome (Orphanet:217346)
1q44 microdeletion syndrome (Orphanet:238769)
2q31.1 microdeletion syndrome (Orphanet:251014)
2q32q33 microdeletion syndrome (Orphanet:251019)
2q37 microdeletion syndrome (Orphanet:1001)
4q21 microdeletion syndrome (Orphanet:238750)
ALG1-CDG (Orphanet:79327)
Ablepharon macrostomia syndrome (Orphanet:920)
Acro-osteolysis-keloid-like lesions-premature aging syndrome (Orphanet:363665)
Acrocallosal syndrome (Orphanet:36)
Acroosteolysis, dominant type (Orphanet:955)
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis (Orphanet:86818)
Arachnodactyly - intellectual deficit - dysmorphism (Orphanet:1130)
Arthrogryposis multiplex congenita - whistling face (Orphanet:1150)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Baraitser-Winter syndrome (Orphanet:2995)
Barber-Say syndrome (Orphanet:1231)
Blepharophimosis-intellectual deficit syndrome, MKB type (Orphanet:293707)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
C syndrome (Orphanet:1308)
CEREBROOCULOFACIOSKELETAL SYNDROME 1 (OMIM:214150)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
COFS syndrome (Orphanet:1466)
CORNELIA DE LANGE SYNDROME 3 (OMIM:610759)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Charlie M syndrome (Orphanet:1406)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Cleft palate - short stature - vertebral anomalies (Orphanet:2015)
Cornelia de Lange syndrome (Orphanet:199)
Cranioectodermal dysplasia 4 (OMIM:614378)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis (Orphanet:171839)
Deafness - onychodystrophy (Orphanet:3231)
Disorder of sex development - intellectual deficit (Orphanet:2983)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal monosomy 3p (Orphanet:1620)
Distal trisomy 6p (Orphanet:1745)
Edinburgh malformation syndrome (Orphanet:1895)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Ellis Van Creveld syndrome (Orphanet:289)
Femoral-facial syndrome (Orphanet:1988)
Fetal alcohol syndrome (Orphanet:1915)
Fetal valproate syndrome (Orphanet:1906)
Filippi syndrome (Orphanet:3255)
Fine-Lubinsky syndrome (Orphanet:1272)
Floating-Harbor syndrome (Orphanet:2044)
GRANDDAD SYNDROME (OMIM:138920)
Geleophysic dysplasia (Orphanet:2623)
Glycogen storage disease due to glycogen debranching enzyme deficiency (Orphanet:366)
Growth delay due to insulin-like growth factor I resistance (Orphanet:73273)
Gómez-López-Hernández syndrome (Orphanet:1532)
Hallermann-Streiff syndrome (Orphanet:2108)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Hypertelorism, Teebi type (Orphanet:1519)
Ichthyosis - oral and digital anomalies (Orphanet:2272)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome (Orphanet:363611)
LIG4 syndrome (Orphanet:99812)
Langer-Giedion syndrome (Orphanet:502)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
Lathosterolosis (Orphanet:46059)
Lethal hemolytic anemia - genital anomalies (Orphanet:1046)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44 (OMIM:615942)
MGAT2-CDG (Orphanet:79329)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
Mesomelic dwarfism - cleft palate - camptodactyly (Orphanet:2631)
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty (Orphanet:2504)
Microcephaly - intellectual deficit - phalangeal and neurological anomalies (Orphanet:137658)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mucopolysaccharidosis type 2 (Orphanet:580)
Multiple congenital anomalies - hypotonia - seizures syndrome (Orphanet:280633)
Myhre syndrome (Orphanet:2588)
Non-distal trisomy 13q (Orphanet:1702)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Norrie disease (Orphanet:649)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
OSTEOGENESIS IMPERFECTA, TYPE XIII (OMIM:614856)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Oculocerebrorenal syndrome (Orphanet:534)
Omphalocele syndrome, Shprintzen-Goldberg type (Orphanet:3164)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
PYCR1-related DeBarsy syndrome (Orphanet:293633)
Paternal 20q13.2q13.3 microdeletion syndrome (Orphanet:261304)
Peters-plus syndrome (Orphanet:709)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Premature chromosome condensation with microcephaly and intellectual deficit (Orphanet:52183)
RHINY (OMIM:180360)
Recombinant 8 syndrome (Orphanet:96167)
Ring chromosome 10 (Orphanet:1438)
Ruvalcaba syndrome (Orphanet:3121)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION (OMIM:612447)
Sanjad-Sakati syndrome (Orphanet:2323)
Schilbach-Rott syndrome (Orphanet:2353)
Silver-Russell syndrome (Orphanet:813)
Spondylo-ocular syndrome (Orphanet:85194)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Tetralogy of Fallot (Orphanet:3303)
Tetrasomy 12p (Orphanet:884)
Tetrasomy 18p (Orphanet:3307)
Toluene embryopathy (Orphanet:1920)
Toriello-Carey syndrome (Orphanet:3338)
Transaldolase deficiency (Orphanet:101028)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Trisomy 20p (Orphanet:261318)
Ulbright-Hodes syndrome (Orphanet:3404)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Xq27.3q28 duplication syndrome (Orphanet:261483)
Yunis-Varon syndrome (Orphanet:3472)