Tented upper lip vermilion
Symptom Information:
Symptom ID: | HPO:0010804 | |||||||
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 upper lip(HPO:0000177) Abnormality of upper lip vermillion(HPO:0011339) Tented upper lip vermilion(HPO:0010804) MedDRA: |
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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) |