Broad forehead

Symptom Information:

Symptom ID: HPO:0000337
Synonyms:
Wide forehead [HPO:0000337]
Broad forehead [OMIM:Broad forehead]
Wide forehead [OMIM:Wide forehead]
Broad forehead [Orphanet:2760]
Broad forehead (2 patients) [OMIM:Broad forehead (2 patients)]
Broad forehead (in some patients) [OMIM:Broad forehead (in some patients)]
Quality:
Cross references:
Orphanet:2760 "Broad forehead" [Orphanet:2760]
OMIM: "Broad forehead" [OMIM:Broad forehead]
OMIM: "Wide forehead" [OMIM:Wide forehead]
OMIM: "Broad forehead (2 patients)" [OMIM:Broad forehead (2 patients)]
OMIM: "Broad forehead (in some patients)" [OMIM:Broad forehead (in some patients)]
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)
                   Broad forehead(HPO:0000337)
MedDRA:
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)