Narrow face
Symptom Information:
Symptom ID: | HPO:0000275 | |||||||||
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) Abnormal facial shape(HPO:0001999) Narrow face(HPO:0000275) MedDRA: |
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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) |