Thick lower lip vermilion
Symptom Information:
Symptom ID: | HPO:0000179 | ||||||
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) Abnormality of lower lip(HPO:0000178) Thick lower lip vermilion(HPO:0000179) Thick vermilion border(HPO:0012471) Thick lower lip vermilion(HPO:0000179) MedDRA: |
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Database Frequency: | 72 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
3M syndrome | (Orphanet:2616) |
48,XXYY syndrome | (Orphanet:10) |
Acromicric dysplasia | (Orphanet:969) |
Alpha-N-acetylgalactosaminidase deficiency type 2 | (Orphanet:79280) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Aspartylglucosaminuria | (Orphanet:93) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal dominant prognathism | (Orphanet:2964) |
Autosomal recessive infantile hypercalcemia | (Orphanet:300547) |
Blepharophimosis - ptosis - esotropia - syndactyly - short stature | (Orphanet:2057) |
CLARK-BARAITSER SYNDROME | (OMIM:300602) |
Cabezas syndrome | (Orphanet:85293) |
Carpenter-Waziri syndrome | (Orphanet:93973) |
Cataract-congenital heart disease-neural tube defect syndrome | (Orphanet:314993) |
Chudley-Lowry-Hoar syndrome | (Orphanet:93971) |
Coffin-Siris syndrome | (Orphanet:1465) |
Costello syndrome | (Orphanet:3071) |
Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Fountain syndrome | (Orphanet:3219) |
Fucosidosis | (Orphanet:349) |
GAPO syndrome | (Orphanet:2067) |
Hall-Riggs syndrome | (Orphanet:2107) |
Holmes-Gang syndrome | (Orphanet:93970) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, X-linked, Shashi type | (Orphanet:85286) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Intellectual deficit, X-linked, Wilson type | (Orphanet:85290) |
Ito hypomelanosis | (Orphanet:435) |
Juberg-Marsidi syndrome | (Orphanet:93972) |
KAHRIZI SYNDROME | (OMIM:612713) |
LEOPARD SYNDROME 2 | (OMIM:611554) |
Leprechaunism | (Orphanet:508) |
MACS syndrome | (Orphanet:217335) |
MEIER-GORLIN SYNDROME 3 | (OMIM:613803) |
MEIER-GORLIN SYNDROME 4 | (OMIM:613804) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 | (OMIM:614607) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 24 | (OMIM:615828) |
MENTAL RETARDATION, X-LINKED 19 | (OMIM:300844) |
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA | (OMIM:608624) |
MOMO syndrome | (Orphanet:2563) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
Marshall syndrome | (Orphanet:560) |
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type | (Orphanet:217026) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
Monosomy 5p | (Orphanet:281) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Multiple endocrine neoplasia type 2B | (Orphanet:247709) |
NOONAN SYNDROME 4 | (OMIM:610733) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Neu-Laxova syndrome | (Orphanet:2671) |
Non-progressive cerebellar ataxia with intellectual deficit | (Orphanet:314647) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY | (OMIM:611087) |
Recombinant 8 syndrome | (Orphanet:96167) |
Renier-Gabreels-Jasper syndrome | (Orphanet:93975) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES | (OMIM:600093) |
Sanfilippo syndrome type D | (Orphanet:79272) |
Smith-Fineman-Myers syndrome | (Orphanet:93974) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
Williams syndrome | (Orphanet:904) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |
Zimmermann-Laband syndrome | (Orphanet:3473) |
Zunich-Kaye syndrome | (Orphanet:3474) |