Broad forehead
Symptom Information:
Symptom ID: | HPO:0000337 | ||||||
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) Broad forehead(HPO:0000337) MedDRA: |
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Database Frequency: | 116 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
10q22.3q23.3 microduplication syndrome | (Orphanet:276422) |
14q11.2 microdeletion syndrome | (Orphanet:261120) |
17p11.2 microduplication syndrome | (Orphanet:1713) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
3C syndrome | (Orphanet:7) |
3M syndrome | (Orphanet:2616) |
3MC SYNDROME 2 | (OMIM:265050) |
4q21 microdeletion syndrome | (Orphanet:238750) |
5p13 microduplication syndrome | (Orphanet:329802) |
5q14.3 microdeletion syndrome | (Orphanet:228384) |
Aarskog-Scott syndrome | (Orphanet:915) |
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
Acrocallosal syndrome | (Orphanet:36) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Acromegaly | (Orphanet:963) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Alagille syndrome due to a NOTCH2 point mutation | (Orphanet:261629) |
Alpha-mannosidosis | (Orphanet:61) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Aortic arch anomaly - peculiar facies - intellectual deficit | (Orphanet:1110) |
Apert syndrome | (Orphanet:87) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
Autosomal recessive cutis laxa type 2B | (Orphanet:357064) |
Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
Baller-Gerold syndrome | (Orphanet:1225) |
Brachytelephalangy - dysmorphism - Kallmann syndrome | (Orphanet:1295) |
CARDIOFACIOCUTANEOUS SYNDROME 2 | (OMIM:615278) |
CHROMOSOME 15q11.2 DELETION SYNDROME | (OMIM:615656) |
CHROMOSOME 1p32-p31 DELETION SYNDROME | (OMIM:613735) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME | (OMIM:218650) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cerebellar ataxia - ectodermal dysplasia | (Orphanet:1174) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Char syndrome | (Orphanet:46627) |
Congenital disorder of glycosylation | (Orphanet:137) |
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
De Barsy syndrome | (Orphanet:2962) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Distal monosomy 6p | (Orphanet:96125) |
Donnai-Barrow syndrome | (Orphanet:2143) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Epimetaphyseal skeletal dysplasia | (Orphanet:1819) |
Facial dysmorphism - immunodeficiency - livedo - short stature | (Orphanet:352712) |
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation | (Orphanet:1970) |
Familial visceral myopathy | (Orphanet:2604) |
Filippi syndrome | (Orphanet:3255) |
Fine-Lubinsky syndrome | (Orphanet:1272) |
Flat face - microstomia - ear anomaly | (Orphanet:1968) |
Fronto-facio-nasal dysostosis | (Orphanet:1791) |
Fryns syndrome | (Orphanet:2059) |
GAPO syndrome | (Orphanet:2067) |
Hennekam syndrome | (Orphanet:2136) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
Intellectual deficit - balding - patella luxation - acromicria | (Orphanet:3041) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Intellectual deficit - short stature - hypertelorism | (Orphanet:3074) |
Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
Intellectual deficit, X-linked, Wittwer type | (Orphanet:85291) |
Isolated brachycephaly | (Orphanet:35099) |
Keipert syndrome | (Orphanet:2662) |
Kleefstra syndrome | (Orphanet:261494) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Large congenital melanocytic nevus | (Orphanet:626) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE | (OMIM:248000) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35 | (OMIM:615162) |
MOMO syndrome | (Orphanet:2563) |
Macrocephaly - short stature - paraplegia | (Orphanet:2427) |
Macrocephaly - spastic paraplegia - dysmorphism | (Orphanet:2429) |
Macrocephaly-autism syndrome | (Orphanet:210548) |
Macrosomia - microphthalmia - cleft palate | (Orphanet:2432) |
Marden-Walker syndrome | (Orphanet:2461) |
Meckel syndrome, type 8 | (OMIM:613885) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Microcephaly - intellectual deficit - phalangeal and neurological anomalies | (Orphanet:137658) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
Monosomy 13q14 | (Orphanet:1587) |
Mulibrey nanism | (Orphanet:2576) |
Nasopalpebral lipoma - coloboma - telecanthus | (Orphanet:2399) |
Noonan syndrome | (Orphanet:648) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
Osteosclerosis - developmental delay - craniosynostosis | (Orphanet:178377) |
Overgrowth - macrocephaly - facial dysmorphism | (Orphanet:137634) |
PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER) | (OMIM:614882) |
Pai syndrome | (Orphanet:1993) |
Pectus excavatum - macrocephaly - dysplastic nails | (Orphanet:2835) |
Polyvalvular heart disease syndrome | (Orphanet:228410) |
Potocki-Shaffer syndrome | (Orphanet:52022) |
Progeroid syndrome, Petty type | (Orphanet:2963) |
Proximal 16p11.2 microdeletion syndrome | (Orphanet:261197) |
SIMOSA CRANIOFACIAL SYNDROME | (OMIM:182150) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Singleton-Merten dysplasia | (Orphanet:85191) |
Smith-Magenis syndrome | (Orphanet:819) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Spondyloepiphyseal dysplasia congenita | (Orphanet:94068) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Tetralogy of Fallot | (Orphanet:3303) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Trisomy 18 | (Orphanet:3380) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay | (Orphanet:73246) |
W syndrome | (Orphanet:2804) |
Weaver syndrome | (Orphanet:3447) |
Williams syndrome | (Orphanet:904) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked intellectual deficit, Najm type | (Orphanet:163937) |