Narrow face

Symptom Information:

Symptom ID: HPO:0000275
Synonyms:
Narrow facies [HPO:0000275]
Thin face [HPO:0000275]
Long face [Orphanet:3220]
Narrow face [OMIM:Narrow face]
Thin face [OMIM:Thin face]
Narrow face [Orphanet:3060]
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)]
Quality:
Cross references:
HPO:0000276 "Long face" [Orphanet:3220]
Orphanet:3220 "Long face" [Orphanet:3220]
Orphanet:3060 "Narrow face" [Orphanet:3060]
OMIM: "Narrow face" [OMIM:Narrow face]
OMIM: "Thin face" [OMIM:Thin 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)]
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)
                   Narrow face(HPO:0000275)
MedDRA:
Database Frequency: 76 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
22q11.2 microduplication syndrome (Orphanet:1727)
2q31.1 microdeletion syndrome (Orphanet:251014)
3q29 microdeletion syndrome (Orphanet:65286)
48,XXYY syndrome (Orphanet:10)
Acro-renal-mandibular syndrome (Orphanet:958)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Arachnodactyly - intellectual deficit - dysmorphism (Orphanet:1130)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive spastic paraplegia type 23 (Orphanet:101003)
BOR syndrome (Orphanet:107)
Baller-Gerold syndrome (Orphanet:1225)
Bangstad syndrome (Orphanet:1227)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
Bloom syndrome (Orphanet:125)
CHARGE syndrome (Orphanet:138)
CK syndrome (Orphanet:251383)
CRANIOACROFACIAL SYNDROME (OMIM:122850)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cap myopathy (Orphanet:171881)
Christianson syndrome (Orphanet:85278)
Congenital fiber-type disproportion myopathy (Orphanet:2020)
Craniofacial-deafness-hand syndrome (Orphanet:1529)
Craniomicromelic syndrome (Orphanet:1524)
Dubowitz syndrome (Orphanet:235)
Dysmorphism - cleft palate - loose skin (Orphanet:1779)
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE (OMIM:608763)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Fetal alcohol syndrome (Orphanet:1915)
Fragile X syndrome (Orphanet:908)
Goldblatt syndrome (Orphanet:166272)
Harrod syndrome (Orphanet:2115)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Koolen-De Vries syndrome (Orphanet:96169)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Lateral meningocele syndrome (Orphanet:2789)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL (OMIM:616313)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION (OMIM:255310)
Marfan syndrome (Orphanet:558)
Marfan syndrome type 1 (Orphanet:284963)
Microbrachycephaly - ptosis - cleft lip (Orphanet:2511)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (Orphanet:369897)
Monosomy 5p (Orphanet:281)
Multiple synostoses syndrome (Orphanet:3237)
Muscular dystrophy - white matter spongiosis (Orphanet:1877)
NEMALINE MYOPATHY 1 (OMIM:609284)
Nance-Horan syndrome (Orphanet:627)
Occipital horn syndrome (Orphanet:198)
Oculo-reno-cerebellar syndrome (Orphanet:2715)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Oculofaciocardiodental syndrome (Orphanet:2712)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Primary dystonia, DYT4 type (Orphanet:98805)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Radio-ulnar synostosis - intellectual deficit - hypotonia (Orphanet:3270)
Renpenning syndrome (Orphanet:3242)
Robin sequence - oligodactyly (Orphanet:3104)
SOTOS SYNDROME 2 (OMIM:614753)
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE (OMIM:613744)
Seckel syndrome (Orphanet:808)
Sheldon-Hall syndrome (Orphanet:1147)
Sillence syndrome (Orphanet:3168)
Summitt syndrome (Orphanet:3210)
Trisomy 18 (Orphanet:3380)
Velo-facial-skeletal syndrome (Orphanet:3424)
W syndrome (Orphanet:2804)
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME (OMIM:602418)
Werner syndrome (Orphanet:902)
Williams syndrome (Orphanet:904)
X-linked centronuclear myopathy (Orphanet:596)
X-linked creatine transporter deficiency (Orphanet:52503)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
X-linked intellectual deficit, Golabi-Ito-Hall type (Orphanet:93947)