Thin vermilion border
Symptom Information:
Symptom ID: | HPO:0000233 | |||||||||||
Synonyms: |
|
|||||||||||
Quality: | ||||||||||||
Cross references: |
|
|||||||||||
Is a (Direct Parents): |
|
|||||||||||
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) |