Narrow mouth
Symptom Information:
Symptom ID: | HPO:0000160 | |||||||||||
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 mouth size(HPO:0011337) Narrow mouth(HPO:0000160) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Musculoskeletal and connective tissue disorders of face, neck and jaw congenital(MedDRA:10028380) Narrow mouth(HPO:0000160) |
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Database Frequency: | 188 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
15q24 microdeletion syndrome | (Orphanet:94065) |
17p13.3 microduplication syndrome | (Orphanet:217385) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
1p36 deletion syndrome | (Orphanet:1606) |
20p12.3 microdeletion syndrome | (Orphanet:261295) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
8q12 microduplication syndrome | (Orphanet:228399) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
ALDH18A1-related De Barsy syndrome | (Orphanet:35664) |
AREDYLD syndrome | (Orphanet:1133) |
ARTHROGRYPOSIS, DISTAL, TYPE 2A | (OMIM:193700) |
ARTHROGRYPOSIS, DISTAL, TYPE 2E | (OMIM:121070) |
AURICULOCONDYLAR SYNDROME 1 | (OMIM:602483) |
AURICULOCONDYLAR SYNDROME 2 | (OMIM:614669) |
Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
Acromicric dysplasia | (Orphanet:969) |
Acroosteolysis, dominant type | (Orphanet:955) |
Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
Antley-Bixler syndrome | (Orphanet:83) |
Aortic arch anomaly - peculiar facies - intellectual deficit | (Orphanet:1110) |
Arachnodactyly - intellectual deficit - dysmorphism | (Orphanet:1130) |
Arthrogryposis multiplex congenita - whistling face | (Orphanet:1150) |
Auriculocondylar syndrome | (Orphanet:137888) |
Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
Autosomal recessive cutis laxa type 2, classic type | (Orphanet:357074) |
Autosomal recessive cutis laxa type 2A | (Orphanet:357058) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Baller-Gerold syndrome | (Orphanet:1225) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
Blepharophimosis-intellectual deficit syndrome, MKB type | (Orphanet:293707) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Blepharophimosis-intellectual deficit syndrome, Verloes type | (Orphanet:293725) |
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:601088) |
CHARGE syndrome | (Orphanet:138) |
CHROMOSOME 1p32-p31 DELETION SYNDROME | (OMIM:613735) |
COLD-INDUCED SWEATING SYNDROME 1 | (OMIM:272430) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Camptodactyly - joint contractures - facial skeletal defects | (Orphanet:1323) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Carney complex-trismus-pseudocamptodactyly syndrome | (Orphanet:319340) |
Charlie M syndrome | (Orphanet:1406) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Chondrodysplasia with joint dislocations, gPAPP type | (Orphanet:280586) |
Cleft palate-lateral synechia syndrome | (Orphanet:2016) |
Cold-induced sweating syndrome | (Orphanet:157820) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Cowden syndrome | (Orphanet:201) |
Craniofacial-deafness-hand syndrome | (Orphanet:1529) |
Craniomicromelic syndrome | (Orphanet:1524) |
Cutis gyrata - acanthosis nigricans - craniosynostosis | (Orphanet:1555) |
Cutis laxa | (Orphanet:209) |
DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
De Barsy syndrome | (Orphanet:2962) |
Desbuquois syndrome | (Orphanet:1425) |
Desmosterolosis | (Orphanet:35107) |
Digitotalar dysmorphism | (Orphanet:1146) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
Distal limb deficiencies - micrognathia syndrome | (Orphanet:1307) |
Distal monosomy 17q | (Orphanet:1597) |
Distal trisomy 6p | (Orphanet:1745) |
Down syndrome | (Orphanet:870) |
Dysmorphism - multiple structural anomalies | (Orphanet:1780) |
Dyssegmental dysplasia, Silverman-Handmaker type | (Orphanet:1865) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 | (OMIM:130070) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Edinburgh malformation syndrome | (Orphanet:1895) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS | (OMIM:227255) |
FETAL AKINESIA DEFORMATION SEQUENCE | (OMIM:208150) |
FIBROCHONDROGENESIS 1 | (OMIM:228520) |
FRONTOOCULAR SYNDROME | (OMIM:605321) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Fetal Gaucher disease | (Orphanet:85212) |
Fetal akinesia deformation sequence | (Orphanet:994) |
Fetal valproate syndrome | (Orphanet:1906) |
Fibrochondrogenesis | (Orphanet:2021) |
Fine-Lubinsky syndrome | (Orphanet:1272) |
Flat face - microstomia - ear anomaly | (Orphanet:1968) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2 | (OMIM:616006) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hamel cerebro-palato-cardiac syndrome | (Orphanet:93946) |
Harrod syndrome | (Orphanet:2115) |
Heart defect - round face - congenital developmental delay | (Orphanet:1355) |
Hennekam syndrome | (Orphanet:2136) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Hunter-McAlpine craniosynostosis | (Orphanet:97340) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
Hypoglossia - hypodactyly | (Orphanet:989) |
Hypomandibular faciocranial dysostosis | (Orphanet:1790) |
Ichthyosis - oral and digital anomalies | (Orphanet:2272) |
Iniencephaly | (Orphanet:63259) |
Intellectual deficit - hypoplastic corpus callosum - preauricular tag | (Orphanet:1495) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
Intellectual deficit, X-linked, Pai type | (Orphanet:85322) |
Isolated congenital hypoglossia/aglossia | (Orphanet:141152) |
KBG syndrome | (Orphanet:2332) |
KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS | (OMIM:245160) |
LAMBOTTE SYNDROME | (OMIM:245552) |
LUBS X-LINKED MENTAL RETARDATION SYNDROME | (OMIM:300260) |
Larsen-like osseous dysplasia - short stature | (Orphanet:2370) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
Lethal Kniest-like dysplasia | (Orphanet:2347) |
Lethal Larsen-like syndrome | (Orphanet:2371) |
Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
Lethal hemolytic anemia - genital anomalies | (Orphanet:1046) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MEIER-GORLIN SYNDROME 2 | (OMIM:613800) |
MEIER-GORLIN SYNDROME 3 | (OMIM:613803) |
MEIER-GORLIN SYNDROME 4 | (OMIM:613804) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 | (OMIM:615834) |
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA | (OMIM:608624) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
MYOPATHY, CENTRONUCLEAR, 5 | (OMIM:615959) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Mandibular hypoplasia-deafness-progeroid syndrome | (Orphanet:363649) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Marden-Walker syndrome | (Orphanet:2461) |
Marfanoid habitus - intellectual deficit, autosomal recessive | (Orphanet:2463) |
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus | (Orphanet:83473) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Microcephaly-microcornea syndrome, Seemanova type | (Orphanet:2528) |
Monosomy 9p | (Orphanet:261112) |
Monosomy 9q22.3 | (Orphanet:77301) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Multiple epiphyseal dysplasia, Beighton type | (Orphanet:166011) |
Myhre syndrome | (Orphanet:2588) |
Neuralgic amyotrophy | (Orphanet:2901) |
Non-progressive cerebellar ataxia with intellectual deficit | (Orphanet:314647) |
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:257850) |
OSTEOGENESIS IMPERFECTA, TYPE XII | (OMIM:613849) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
Osteocraniostenosis | (Orphanet:2763) |
Otopalatodigital syndrome | (Orphanet:669) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES | (OMIM:602249) |
Proteus-like syndrome | (Orphanet:2969) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
Renpenning syndrome | (Orphanet:3242) |
Richieri Costa-Pereira syndrome | (Orphanet:3102) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
Ruvalcaba syndrome | (Orphanet:3121) |
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES | (OMIM:602471) |
SIMOSA CRANIOFACIAL SYNDROME | (OMIM:182150) |
SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION | (OMIM:612447) |
STEVENSON-CAREY SYNDROME | (OMIM:611961) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Scleroderma | (Orphanet:801) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Short stature - craniofacial anomalies - genital hypoplasia | (Orphanet:2994) |
Subaortic stenosis - short stature | (Orphanet:3191) |
Syndromic diarrhea | (Orphanet:84064) |
Syngnathia multiple anomalies | (Orphanet:3262) |
Teebi-Shaltout syndrome | (Orphanet:3291) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Tetraamelia - multiple malformations | (Orphanet:3301) |
Tetrasomy 18p | (Orphanet:3307) |
Treacher-Collins syndrome | (Orphanet:861) |
Triploidy | (Orphanet:3376) |
Trisomy 17p | (Orphanet:261290) |
Trisomy 18 | (Orphanet:3380) |
Trisomy 1q | (Orphanet:261344) |
Ulbright-Hodes syndrome | (Orphanet:3404) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
WARBURG MICRO SYNDROME 4 | (OMIM:615663) |
WHISTLING FACE SYNDROME, RECESSIVE FORM | (OMIM:277720) |
Weaver-Williams syndrome | (Orphanet:3448) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Wilson-Turner syndrome | (Orphanet:3459) |
XK aprosencephaly | (Orphanet:3469) |