Narrow forehead

Symptom Information:

Symptom ID: HPO:0000341
Synonyms:
Bitemporal narrowing [HPO:0000341]
Bitemporal narrowness [HPO:0000341]
Bitemporal skull narrowing [HPO:0000341]
Intertemporal narrowing [HPO:0000341]
Narrow bitemporal diameter [HPO:0000341]
Temporal narrowness [HPO:0000341]
Bitemporal narrowing [OMIM:Bitemporal narrowing]
Narrow bitemporal diameter [OMIM:Narrow bitemporal diameter]
Narrow forehead [OMIM:Narrow forehead]
Narrow forehead [Orphanet:2800]
Bitemporal narrowing (2 patients) [OMIM:Bitemporal narrowing (2 patients)]
Bitemporal narrowing (53%) [OMIM:Bitemporal narrowing (53%)]
Quality:
Cross references:
HPO:0004422 "Biparietal narrowing" [Orphanet:2800]
Orphanet:2800 "Narrow forehead" [Orphanet:2800]
OMIM: "Bitemporal narrowing" [OMIM:Bitemporal narrowing]
OMIM: "Narrow bitemporal diameter" [OMIM:Narrow bitemporal diameter]
OMIM: "Narrow forehead" [OMIM:Narrow forehead]
OMIM: "Bitemporal narrowing (2 patients)" [OMIM:Bitemporal narrowing (2 patients)]
OMIM: "Bitemporal narrowing (53%)" [OMIM:Bitemporal narrowing (53%)]
Is a (Direct Parents):
Orphanet Abnormality of the skull
HPO         Abnormality of the forehead
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 forehead(HPO:0000290)
                   Narrow forehead(HPO:0000341)
MedDRA:
Database Frequency: 96 / 7739
Resource:

All diseases associated with this symptom:

15q14 microdeletion syndrome (Orphanet:261190)
16q24.3 microdeletion syndrome (Orphanet:261250)
1q44 microdeletion syndrome (Orphanet:238769)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
3q29 microduplication (Orphanet:251038)
5p13 microduplication syndrome (Orphanet:329802)
8p23.1 microdeletion syndrome (Orphanet:251071)
8q22.1 microdeletion syndrome (Orphanet:178303)
Acro-oto-ocular syndrome (Orphanet:2980)
Adenylosuccinate lyase deficiency (Orphanet:46)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Autosomal recessive chorioretinopathy-microcephaly (Orphanet:2518)
Bohring-Opitz syndrome (Orphanet:97297)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
C syndrome (Orphanet:1308)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
CORNELIA DE LANGE SYNDROME 2 (OMIM:300590)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carpenter-Waziri syndrome (Orphanet:93973)
Cerebro-facio-articular syndrome (Orphanet:314679)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
Craniofacial dyssynostosis (Orphanet:1516)
Deafness - onychodystrophy (Orphanet:3231)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 (OMIM:615859)
Fetal alcohol syndrome (Orphanet:1915)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
HOLOPROSENCEPHALY 5 (OMIM:609637)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
Hepatic fibrosis - renal cysts - intellectual deficit (Orphanet:2031)
Holmes-Gang syndrome (Orphanet:93970)
Insulin-resistance syndrome type A (Orphanet:2297)
Intellectual deficit, Birk-Barel type (Orphanet:166108)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
Isotretinoin syndrome (Orphanet:2305)
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)
Juberg-Marsidi syndrome (Orphanet:93972)
LIG4 syndrome (Orphanet:99812)
Lathosterolosis (Orphanet:46059)
Linear nevus sebaceus syndrome (Orphanet:2612)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 (OMIM:616268)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 7 (OMIM:614104)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III (OMIM:210730)
MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLARATROPHY (OMIM:615760)
Microbrachycephaly - ptosis - cleft lip (Orphanet:2511)
Mikati-Najjar-Sahli syndrome (Orphanet:2558)
Mosaic trisomy 9 (Orphanet:99776)
Mucolipidosis type 2 (Orphanet:576)
Mucolipidosis type 4 (Orphanet:578)
Multiple congenital anomalies - hypotonia - seizures syndrome (Orphanet:280633)
Non-distal monosomy 10q (Orphanet:1581)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
PEHO syndrome (Orphanet:2836)
PEHO-like syndrome (Orphanet:99807)
Pitt-Hopkins syndrome (Orphanet:2896)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Prader-Willi syndrome (Orphanet:739)
Pseudoaminopterin syndrome (Orphanet:221120)
Pterygium colli - intellectual deficit - digital anomalies (Orphanet:2988)
Ptosis - upper ocular movement limitation - absence of lacrimal punctum (Orphanet:228396)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
SCHAAF-YANG SYNDROME (OMIM:615547)
SECKEL SYNDROME 2 (OMIM:606744)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
SHORT STATURE-OBESITY SYNDROME (OMIM:269870)
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE (OMIM:614066)
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE (OMIM:613744)
Schinzel-Giedion syndrome (Orphanet:798)
Severe intellectual deficit and progressive spastic paraplegia (Orphanet:280763)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Teebi-Shaltout syndrome (Orphanet:3291)
Tetraploidy (Orphanet:3305)
Toluene embryopathy (Orphanet:1920)
Trichodental syndrome (Orphanet:3351)
Trigonocephaly - bifid nose - acral anomalies (Orphanet:3368)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
VERHEIJ SYNDROME (OMIM:615583)
Williams syndrome (Orphanet:904)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)