Preauricular skin tag
Symptom Information:
Symptom ID: | HPO:0000384 | |||||||||||||||
Synonyms: |
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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 the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Localized skin lesion(HPO:0011355) Skin tags(HPO:0010609) Preauricular skin tag(HPO:0000384) Abnormality of the ear(HPO:0000598) Abnormality of the outer ear(HPO:0000356) Abnormality of periauricular region(HPO:0000383) Preauricular skin tag(HPO:0000384) MedDRA: |
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Database Frequency: | 62 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
16p13.11 microdeletion syndrome | (Orphanet:261236) |
16q24.3 microdeletion syndrome | (Orphanet:261250) |
1q41q42 microdeletion syndrome | (Orphanet:250999) |
1q44 microdeletion syndrome | (Orphanet:238769) |
3C syndrome | (Orphanet:7) |
Acrocallosal syndrome | (Orphanet:36) |
Auriculocondylar syndrome | (Orphanet:137888) |
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
BOR syndrome | (Orphanet:107) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
BRANCHIOOTIC SYNDROME 3 | (OMIM:608389) |
BRANCHIOOTORENAL SYNDROME 2 | (OMIM:610896) |
Branchio-otic syndrome | (Orphanet:52429) |
Branchiogenic deafness syndrome | (Orphanet:50815) |
CHARGE syndrome | (Orphanet:138) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CORPUS CALLOSUM, AGENESIS OF | (OMIM:217990) |
Cat-eye syndrome | (Orphanet:195) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cohen syndrome | (Orphanet:193) |
Conductive deafness - malformed external ear | (Orphanet:3216) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniotelencephalic dysplasia | (Orphanet:1528) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
Emanuel syndrome | (Orphanet:96170) |
Fronto-facio-nasal dysostosis | (Orphanet:1791) |
Frontonasal dysplasia | (Orphanet:250) |
Goldenhar syndrome | (Orphanet:374) |
Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
Intellectual deficit - hypoplastic corpus callosum - preauricular tag | (Orphanet:1495) |
Isolated trigonocephaly | (Orphanet:3366) |
Isotretinoin-like syndrome | (Orphanet:2306) |
Kabuki syndrome | (Orphanet:2322) |
Kapur-Toriello syndrome | (Orphanet:2328) |
Lambert syndrome | (Orphanet:1296) |
Lowe-Kohn-Cohen syndrome | (Orphanet:2408) |
Lowry-MacLean syndrome | (Orphanet:2409) |
Macrostomia - preauricular tags - external ophthalmoplegia | (Orphanet:83619) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Microcephaly - deafness - intellectual deficit | (Orphanet:2533) |
Microphthalmia - ankyloblepharon - intellectual deficit | (Orphanet:85275) |
Microphthalmia, Lenz type | (Orphanet:568) |
Monosomy 5p | (Orphanet:281) |
Nager syndrome | (Orphanet:245) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Oculocerebrocutaneous syndrome | (Orphanet:1647) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
PREAURICULAR TAG, ISOLATED, AUTOSOMAL DOMINANT, 1 | (OMIM:610420) |
Peters-plus syndrome | (Orphanet:709) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Spondylocarpotarsal synostosis | (Orphanet:3275) |
TRIGONOCEPHALY 1 | (OMIM:190440) |
TRISOMY 18-LIKE SYNDROME | (OMIM:601161) |
Tetraploidy | (Orphanet:3305) |
Townes-Brocks syndrome | (Orphanet:857) |
Treacher-Collins syndrome | (Orphanet:861) |
Trisomy 13 | (Orphanet:3378) |
Wildervanck syndrome | (Orphanet:3456) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |