Everted lower lip vermilion
Symptom Information:
Symptom ID: | HPO:0000232 | ||||||||||
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) Eclabion(HPO:0012472) Everted lower lip vermilion(HPO:0000232) Abnormality of lower lip(HPO:0000178) Everted lower lip vermilion(HPO:0000232) MedDRA: |
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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) |