Long face

Symptom Information:

Symptom ID: HPO:0000276
Synonyms:
Long mid-face [Orphanet:3500]
Long face [OMIM:Long face]
Long face [Orphanet:3220]
Long midface [Orphanet:3500]
Long face (1 patient) [OMIM:Long face (1 patient)]
Long face (74%) [OMIM:Long face (74%)]
Long face (in 1/4 patients) [OMIM:Long face (in 1/4 patients)]
Long midface [OMIM:Long midface]
Quality:
Cross references:
HPO:0000275 "Narrow face" [Orphanet:3220]
Orphanet:3220 "Long face" [Orphanet:3220]
Orphanet:3500 "Long midface" [Orphanet:3500]
OMIM: "Long face" [OMIM:Long face]
OMIM: "Long face (1 patient)" [OMIM:Long face (1 patient)]
OMIM: "Long face (74%)" [OMIM:Long face (74%)]
OMIM: "Long face (in 1/4 patients)" [OMIM:Long face (in 1/4 patients)]
OMIM: "Long midface" [OMIM:Long midface]
Is a (Direct Parents):
HPO         Abnormal facial shape
Orphanet Abnormal facial shape
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:
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)