Tented upper lip vermilion

Symptom Information:

Symptom ID: HPO:0010804
Synonyms:
Inverted V-shaped upper lip [HPO:0010804]
Tented mouth [HPO:0010804]
Inverted V-shaped upper lip [OMIM:Inverted V-shaped upper lip]
Tented mouth [OMIM:Tented mouth]
Tented upper lip [Orphanet:9280]
Tented upper lip [OMIM:Tented upper lip]
Tented upper lip (HCS) [OMIM:Tented upper lip (HCS)]
Quality:
Cross references:
Orphanet:9280 "Tented upper lip" [Orphanet:9280]
OMIM: "Inverted V-shaped upper lip" [OMIM:Inverted V-shaped upper lip]
OMIM: "Tented mouth" [OMIM:Tented mouth]
OMIM: "Tented upper lip" [OMIM:Tented upper lip]
OMIM: "Tented upper lip (HCS)" [OMIM:Tented upper lip (HCS)]
Is a (Direct Parents):
HPO         Abnormality of upper lip vermillion
Orphanet Abnormality of the mouth
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 upper lip(HPO:0000177)
                         Abnormality of upper lip vermillion(HPO:0011339)
                            Tented upper lip vermilion(HPO:0010804)
MedDRA:
Database Frequency: 47 / 7739
Resource:

All diseases associated with this symptom:

14q12 microdeletion syndrome (Orphanet:261144)
2p21 microdeletion syndrome (Orphanet:163693)
2q23.1 microdeletion syndrome (Orphanet:228402)
Atypical hypotonia - cystinuria syndrome (Orphanet:238523)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
CHROMOSOME 15q25 DELETION SYNDROME (OMIM:614294)
Carpenter-Waziri syndrome (Orphanet:93973)
Cerebro-facio-articular syndrome (Orphanet:314679)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Distal monosomy 6p (Orphanet:96125)
Dysmorphism - pectus carinatum - joint laxity (Orphanet:2104)
Fryns syndrome (Orphanet:2059)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 (OMIM:614749)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4 (OMIM:615716)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 5 (OMIM:616025)
Holmes-Gang syndrome (Orphanet:93970)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Intellectual deficit, X-linked, Cantagrel type (Orphanet:85277)
Intellectual deficit, X-linked, Stevenson type (Orphanet:85325)
Joubert syndrome 14 (OMIM:614424)
Juberg-Marsidi syndrome (Orphanet:93972)
KEPPEN-LUBINSKY SYNDROME (OMIM:614098)
Keipert syndrome (Orphanet:2662)
Kleefstra syndrome (Orphanet:261494)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY (OMIM:606369)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 24 (OMIM:615828)
MENTAL RETARDATION, X-LINKED 21 (OMIM:300143)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Okamoto syndrome (Orphanet:2729)
Osteocraniostenosis (Orphanet:2763)
PEHO syndrome (Orphanet:2836)
PEHO-like syndrome (Orphanet:99807)
Perlman syndrome (Orphanet:2849)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Magenis syndrome (Orphanet:819)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Trisomy Xq28 (Orphanet:1762)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Waardenburg syndrome type 1 (Orphanet:894)
Waardenburg syndrome type 3 (Orphanet:896)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)