Narrow forehead
Symptom Information:
Symptom ID: | HPO:0000341 | ||||||||||||
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) Abnormality of the forehead(HPO:0000290) Narrow forehead(HPO:0000341) MedDRA: |
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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) |