Preauricular pit
Symptom Information:
Symptom ID: | HPO:0004467 | ||||||||||||||||||||||||||||||||
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 the ear(HPO:0000598) Abnormality of the outer ear(HPO:0000356) Abnormality of periauricular region(HPO:0000383) Periauricular skin pits(HPO:0100277) Preauricular pit(HPO:0004467) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Localized skin lesion(HPO:0011355) Skin pit(HPO:0100276) Periauricular skin pits(HPO:0100277) Preauricular pit(HPO:0004467) MedDRA: |
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Database Frequency: | 39 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acrocraniofacial dysostosis | (Orphanet:949) |
BOR syndrome | (Orphanet:107) |
BRANCHIOOTIC SYNDROME 1 | (OMIM:602588) |
BRANCHIOOTIC SYNDROME 2 | (OMIM:120502) |
BRANCHIOOTIC SYNDROME 3 | (OMIM:608389) |
BRANCHIOOTORENAL SYNDROME 1 | (OMIM:113650) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
Branchio-otic syndrome | (Orphanet:52429) |
Branchiogenic deafness syndrome | (Orphanet:50815) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CHROMOSOME 17p13.1 DELETION SYNDROME | (OMIM:613776) |
COMMISSURAL LIP PITS | (OMIM:120500) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Carpenter syndrome | (Orphanet:65759) |
Cat-eye syndrome | (Orphanet:195) |
DEAFNESS, AUTOSOMAL DOMINANT 23 | (OMIM:605192) |
Distal monosomy 3p | (Orphanet:1620) |
Emanuel syndrome | (Orphanet:96170) |
GMS syndrome | (Orphanet:2090) |
Goldenhar syndrome | (Orphanet:374) |
Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
Hypertelorism-preauricular sinus-punctual pits-deafness syndrome | (Orphanet:293958) |
KABUKI SYNDROME 1 | (OMIM:147920) |
Kabuki syndrome | (Orphanet:2322) |
Lowry-MacLean syndrome | (Orphanet:2409) |
Microcephaly - cardiac defect - lung malsegmentation | (Orphanet:2516) |
OTOFACIOCERVICAL SYNDROME 1 | (OMIM:166780) |
OTOFACIOCERVICAL SYNDROME 2 | (OMIM:615560) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Otofaciocervical syndrome | (Orphanet:2792) |
PREAURICULAR FISTULAE, CONGENITAL | (OMIM:128700) |
Peters-plus syndrome | (Orphanet:709) |
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES | (OMIM:602471) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES | (OMIM:273390) |
Tetralogy of Fallot | (Orphanet:3303) |
Townes-Brocks syndrome | (Orphanet:857) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |