Everted lower lip vermilion

Symptom Information:

Symptom ID: HPO:0000232
Synonyms:
Drooping lower lip [HPO:0000232]
Everted lower lip [HPO:0000232]
Everted prominent lower lip [HPO:0000232]
Protruding lower lip [HPO:0000232]
Everted lower lip [OMIM:Everted lower lip]
Everted prominent lower lip [OMIM:Everted prominent lower lip]
Protruding lower lip [OMIM:Protruding lower lip]
Everted lower lip [Orphanet:9240]
Everted lower lip (in some patients) [OMIM:Everted lower lip (in some patients)]
Lower lip droop [OMIM:Lower lip droop]
Quality:
Cross references:
Orphanet:9240 "Everted lower lip" [Orphanet:9240]
OMIM: "Everted lower lip" [OMIM:Everted lower lip]
OMIM: "Everted prominent lower lip" [OMIM:Everted prominent lower lip]
OMIM: "Protruding lower lip" [OMIM:Protruding lower lip]
OMIM: "Everted lower lip (in some patients)" [OMIM:Everted lower lip (in some patients)]
OMIM: "Lower lip droop" [OMIM:Lower lip droop]
Is a (Direct Parents):
HPO         Eclabion
HPO         Abnormality of lower lip
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)
                      Eclabion(HPO:0012472)
                         Everted lower lip vermilion(HPO:0000232)
                      Abnormality of lower lip(HPO:0000178)
                         Everted lower lip vermilion(HPO:0000232)
MedDRA:
Database Frequency: 90 / 7739
Resource:

All diseases associated with this symptom:

14q11.2 microdeletion syndrome (Orphanet:261120)
14q12 microdeletion syndrome (Orphanet:261144)
15q24 microdeletion syndrome (Orphanet:94065)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q23.1 microdeletion syndrome (Orphanet:228402)
2q31.1 microdeletion syndrome (Orphanet:251014)
3q29 microdeletion syndrome (Orphanet:65286)
8q12 microduplication syndrome (Orphanet:228399)
AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
Aarskog-Scott syndrome (Orphanet:915)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Amelo-onycho-hypohidrotic syndrome (Orphanet:1028)
Autosomal dominant prognathism (Orphanet:2964)
Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
Axenfeld-Rieger syndrome (Orphanet:782)
Bathing suit ichthyosis (Orphanet:100976)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Brain malformation - congenital heart disease - postaxial polydactyly (Orphanet:75389)
Cabezas syndrome (Orphanet:85293)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Char syndrome (Orphanet:46627)
Cheilitis glandularis (Orphanet:1221)
Coffin-Lowry syndrome (Orphanet:192)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cranioectodermal dysplasia 2 (OMIM:613610)
Cranioectodermal dysplasia 3 (OMIM:614099)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Deafness - onychodystrophy (Orphanet:3231)
Dorfman-Chanarin disease (Orphanet:98907)
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALDOMINANT (OMIM:614940)
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:614941)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Feingold syndrome (Orphanet:1305)
Fetal Gaucher disease (Orphanet:85212)
Fountain syndrome (Orphanet:3219)
Fryns-Smeets-Thiry syndrome (Orphanet:2058)
GAPO syndrome (Orphanet:2067)
Gingival fibromatosis - facial dysmorphism (Orphanet:2025)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Growth delay due to insulin-like growth factor I resistance (Orphanet:73273)
Growth hormone insensitivity syndrome (Orphanet:181393)
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES (OMIM:609943)
Hallermann-Streiff syndrome (Orphanet:2108)
Harlequin ichthyosis (Orphanet:457)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Hypertelorism, Teebi type (Orphanet:1519)
Hypodontia - dysplasia of nails (Orphanet:2228)
Hypospadias - hypertelorism - coloboma and deafness (Orphanet:157788)
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit (Orphanet:2269)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Kleefstra syndrome (Orphanet:261494)
Kleefstra syndrome due to 9q34 microdeletion (Orphanet:96147)
Koolen-De Vries syndrome (Orphanet:96169)
Lamellar ichthyosis (Orphanet:313)
Large congenital melanocytic nevus (Orphanet:626)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35 (OMIM:615162)
MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION (OMIM:249670)
MGAT2-CDG (Orphanet:79329)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 (OMIM:253280)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Microcephaly - deafness - intellectual deficit (Orphanet:2533)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (Orphanet:369897)
Monosomy 13q14 (Orphanet:1587)
Mowat-Wilson syndrome (Orphanet:2152)
Neu-Laxova syndrome (Orphanet:2671)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Non-distal trisomy 13q (Orphanet:1702)
Okamoto syndrome (Orphanet:2729)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Pachygyria - epilepsy - intellectual deficit - dysmorphism (Orphanet:94084)
Progeroid syndrome, Petty type (Orphanet:2963)
Sanfilippo syndrome type C (Orphanet:79271)
Self-healing collodion baby (Orphanet:281122)
Symptomatic form of Coffin-Lowry syndrome in female carriers (Orphanet:276630)
Tetrasomy 12p (Orphanet:884)
Trisomy 12p (Orphanet:1699)
Trisomy 20p (Orphanet:261318)
Trisomy 8q (Orphanet:1752)
Trisomy Xq28 (Orphanet:1762)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Van den Ende-Gupta syndrome (Orphanet:2460)
Williams syndrome (Orphanet:904)
Wilson-Turner syndrome (Orphanet:3459)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)