Downturned corners of mouth
Symptom Information:
Symptom ID: | HPO:0002714 | ||||||||
Synonyms: |
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Quality: | |||||||||
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 mouth shape(HPO:0011338) Downturned corners of mouth(HPO:0002714) MedDRA: |
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Database Frequency: | 98 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
12q14 microdeletion syndrome | (Orphanet:94063) |
14q22q23 microdeletion syndrome | (Orphanet:264200) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
2q31.1 microdeletion syndrome | (Orphanet:251014) |
2q37 microdeletion syndrome | (Orphanet:1001) |
3MC SYNDROME 2 | (OMIM:265050) |
4q21 microdeletion syndrome | (Orphanet:238750) |
5q14.3 microdeletion syndrome | (Orphanet:228384) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
Acroosteolysis, dominant type | (Orphanet:955) |
Aniridia - renal agenesis - psychomotor retardation | (Orphanet:1064) |
Aortic arch anomaly - peculiar facies - intellectual deficit | (Orphanet:1110) |
Arthrogryposis multiplex congenita - whistling face | (Orphanet:1150) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive deafness-onychodystrophy syndrome | (Orphanet:79500) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
CORNELIA DE LANGE SYNDROME 2 | (OMIM:300590) |
CORNELIA DE LANGE SYNDROME 5 | (OMIM:300882) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Cerebro-facio-articular syndrome | (Orphanet:314679) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Cerebro-reno-digital syndrome | (Orphanet:1396) |
Cloverleaf skull - multiple congenital anomalies | (Orphanet:93267) |
Connective tissue disorder due to lysyl hydroxylase-3 deficiency | (Orphanet:300284) |
Cornelia de Lange syndrome | (Orphanet:199) |
DEND syndrome | (Orphanet:79134) |
Disorder of sex development - intellectual deficit | (Orphanet:2983) |
Distal monosomy 3p | (Orphanet:1620) |
Distal monosomy 6p | (Orphanet:96125) |
Distal trisomy 15q | (Orphanet:1707) |
Down syndrome | (Orphanet:870) |
Dysmorphism - multiple structural anomalies | (Orphanet:1780) |
Edinburgh malformation syndrome | (Orphanet:1895) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS | (OMIM:227255) |
Facial ectodermal dysplasia | (Orphanet:1807) |
Familial lambdoid synostosis | (Orphanet:3267) |
Fetal valproate syndrome | (Orphanet:1906) |
Flat face - microstomia - ear anomaly | (Orphanet:1968) |
Floating-Harbor syndrome | (Orphanet:2044) |
Fryns-Smeets-Thiry syndrome | (Orphanet:2058) |
Genito-palato-cardiac syndrome | (Orphanet:2075) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hunter-McAlpine craniosynostosis | (Orphanet:97340) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Intellectual deficit, X-linked - cubitus valgus - dysmorphism | (Orphanet:85280) |
Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
Intellectual deficit, X-linked, Nascimento type | (Orphanet:163956) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Kleefstra syndrome | (Orphanet:261494) |
Kleefstra syndrome due to 9q34 microdeletion | (Orphanet:96147) |
Lathosterolosis | (Orphanet:46059) |
Laurin-Sandrow syndrome | (Orphanet:2378) |
Lichstenstein syndrome | (Orphanet:2390) |
MEHMO syndrome | (Orphanet:85282) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 | (OMIM:616268) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13 | (OMIM:613192) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Microcephalic primordial dwarfism, Toriello type | (Orphanet:2643) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Monosomy 18p | (Orphanet:1598) |
Monosomy 18q | (Orphanet:1600) |
Monosomy 5p | (Orphanet:281) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Native American myopathy | (Orphanet:168572) |
Okamoto syndrome | (Orphanet:2729) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Permanent neonatal diabetes mellitus | (Orphanet:99885) |
Pontocerebellar hypoplasia type 3 | (Orphanet:97249) |
Potocki-Shaffer syndrome | (Orphanet:52022) |
Prader-Willi syndrome | (Orphanet:739) |
Radio-renal syndrome | (Orphanet:3015) |
Recombinant 8 syndrome | (Orphanet:96167) |
Ring chromosome 1 | (Orphanet:1437) |
SILVER-RUSSELL SYNDROME | (OMIM:180860) |
STEVENSON-CAREY SYNDROME | (OMIM:611961) |
Severe intellectual deficit - epilepsy - anal anomalies - distal phalangeal hypoplasia | (Orphanet:94066) |
Short stature - heart defect - craniofacial anomalies | (Orphanet:1088) |
Silver-Russell syndrome | (Orphanet:813) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
TEMPLE-BARAITSER SYNDROME | (OMIM:611816) |
TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES | (OMIM:273390) |
Tetrasomy 12p | (Orphanet:884) |
Toriello-Carey syndrome | (Orphanet:3338) |
Trisomy 12p | (Orphanet:1699) |
Trisomy 20p | (Orphanet:261318) |
Trisomy 9p | (Orphanet:236) |
VAN MALDERGEM SYNDROME 1 | (OMIM:601390) |
VAN MALDERGEM SYNDROME 2 | (OMIM:615546) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
WARBURG MICRO SYNDROME 3 | (OMIM:614222) |
Weaver-Williams syndrome | (Orphanet:3448) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |