Thick lower lip vermilion

Symptom Information:

Symptom ID: HPO:0000179
Synonyms:
Full lower lip [HPO:0000179]
Prominent lower lip [HPO:0000179]
Thick lower lip [HPO:0000179]
Full lower lip [OMIM:Full lower lip]
Prominent lower lip [OMIM:Prominent lower lip]
Thick lower lip [OMIM:Thick lower lip]
Quality:
Cross references:
OMIM: "Full lower lip" [OMIM:Full lower lip]
OMIM: "Prominent lower lip" [OMIM:Prominent lower lip]
OMIM: "Thick lower lip" [OMIM:Thick lower lip]
Is a (Direct Parents):
HPO         Abnormality of lower lip
HPO         Thick vermilion border
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:
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)