Thick upper lip vermilion
Symptom Information:
Symptom ID: | HPO:0000215 | |||||||
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 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) Thick vermilion border(HPO:0012471) Thick upper lip vermilion(HPO:0000215) Abnormality of upper lip(HPO:0000177) Abnormality of upper lip vermillion(HPO:0011339) Thick upper lip vermilion(HPO:0000215) MedDRA: |
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Database Frequency: | 17 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
Costello syndrome | (Orphanet:3071) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Intellectual deficit, X-linked, Wilson type | (Orphanet:85290) |
Keipert syndrome | (Orphanet:2662) |
Late-onset localized junctional epidermolysis bullosa - intellectual deficit | (Orphanet:231556) |
Lathosterolosis | (Orphanet:46059) |
Leprechaunism | (Orphanet:508) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Marshall syndrome | (Orphanet:560) |
Miller-Dieker syndrome | (Orphanet:531) |
Multiple synostoses syndrome | (Orphanet:3237) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY | (OMIM:611087) |
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome | (Orphanet:276432) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES | (OMIM:600093) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |