Long face
Symptom Information:
Symptom ID: | HPO:0000276 | ||||||||
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) Abnormal facial shape(HPO:0001999) Long face(HPO:0000276) MedDRA: |
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Database Frequency: | 109 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
15q14 microdeletion syndrome | (Orphanet:261190) |
15q24 microdeletion syndrome | (Orphanet:94065) |
16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
16p13.3 microduplication syndrome | (Orphanet:96078) |
16q24.3 microdeletion syndrome | (Orphanet:261250) |
17q11.2 microduplication syndrome | (Orphanet:139474) |
19q13.11 microdeletion syndrome | (Orphanet:217346) |
22q11.2 deletion syndrome | (Orphanet:567) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
3q29 microdeletion syndrome | (Orphanet:65286) |
3q29 microduplication | (Orphanet:251038) |
48,XXYY syndrome | (Orphanet:10) |
Arachnodactyly - intellectual deficit - dysmorphism | (Orphanet:1130) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
BOR syndrome | (Orphanet:107) |
Bangstad syndrome | (Orphanet:1227) |
Bloom syndrome | (Orphanet:125) |
Bohring-Opitz syndrome | (Orphanet:97297) |
CEDNIK syndrome | (Orphanet:66631) |
CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME | (OMIM:613603) |
CK syndrome | (Orphanet:251383) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Cap myopathy | (Orphanet:171881) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Christianson syndrome | (Orphanet:85278) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Cystic fibrosis - gastritis - megaloblastic anemia | (Orphanet:2575) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
Distal monosomy 19p13.3 | (Orphanet:96129) |
Dysmorphism - cleft palate - loose skin | (Orphanet:1779) |
ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609944) |
Flat face - microstomia - ear anomaly | (Orphanet:1968) |
Fragile X syndrome | (Orphanet:908) |
Fried syndrome | (Orphanet:85335) |
GIACHETI SYNDROME | (OMIM:612917) |
Harrod syndrome | (Orphanet:2115) |
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus | (Orphanet:3044) |
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures | (Orphanet:1568) |
Intellectual deficit, X-linked - hypotonia - facial dysmorphism - aggressive behavior | (Orphanet:85329) |
Intellectual deficit, X-linked, Siderius type | (Orphanet:85287) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Joubert syndrome with ocular defect | (Orphanet:220493) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Joubert syndrome with renal defect | (Orphanet:220497) |
Keutel syndrome | (Orphanet:85202) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY,AND SHORT STATURE | (OMIM:609037) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 | (OMIM:616078) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 | (OMIM:614202) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 | (OMIM:611091) |
MENTAL RETARDATION, X-LINKED 101 | (OMIM:300928) |
MENTAL RETARDATION, X-LINKED 72 | (OMIM:300271) |
MENTAL RETARDATION, X-LINKED 93 | (OMIM:300659) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 | (OMIM:614114) |
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:616326) |
MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL | (OMIM:616313) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
Marfan syndrome type 1 | (Orphanet:284963) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Microbrachycephaly - ptosis - cleft lip | (Orphanet:2511) |
Monosomy 5p | (Orphanet:281) |
Mosaic trisomy 8 | (Orphanet:96061) |
Mowat-Wilson syndrome | (Orphanet:2152) |
NEMALINE MYOPATHY 1 | (OMIM:609284) |
Nance-Horan syndrome | (Orphanet:627) |
Non-progressive cerebellar ataxia with intellectual deficit | (Orphanet:314647) |
OTOFACIOCERVICAL SYNDROME 1 | (OMIM:166780) |
Occipital horn syndrome | (Orphanet:198) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Oculootodental syndrome | (Orphanet:99806) |
Otodental syndrome | (Orphanet:2791) |
Otofaciocervical syndrome | (Orphanet:2792) |
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY | (OMIM:611087) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Polyvalvular heart disease syndrome | (Orphanet:228410) |
Proteus syndrome | (Orphanet:744) |
RAPADILINO syndrome | (Orphanet:3021) |
RIENHOFF SYNDROME | (OMIM:615582) |
Radio-ulnar synostosis - intellectual deficit - hypotonia | (Orphanet:3270) |
Renpenning syndrome | (Orphanet:3242) |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY | (OMIM:614800) |
SIMOSA CRANIOFACIAL SYNDROME | (OMIM:182150) |
SOTOS SYNDROME 2 | (OMIM:614753) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |
Temtamy syndrome | (Orphanet:1777) |
Velo-facial-skeletal syndrome | (Orphanet:3424) |
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME | (OMIM:602418) |
Werner syndrome | (Orphanet:902) |
X-linked centronuclear myopathy | (Orphanet:596) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked intellectual deficit - cerebellar hypoplasia | (Orphanet:137831) |
X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
X-linked intellectual deficit, Golabi-Ito-Hall type | (Orphanet:93947) |