Prominent forehead

Symptom Information:

Symptom ID: HPO:0011220
Synonyms:
Bulging forehead [HPO:0011220]
Bulging forehead [OMIM:Bulging forehead]
Prominent forehead [OMIM:Prominent forehead]
Frontal bossing/prominent forehead [Orphanet:2640]
Bulging forehead (rare) [OMIM:Bulging forehead (rare)]
Forehead prominent [OMIM:Forehead prominent]
Prominent forehead (homozygote) [OMIM:Prominent forehead (homozygote)]
Prominent forehead (in some patients) [OMIM:Prominent forehead (in some patients)]
Prominent forehead (major feature) [OMIM:Prominent forehead (major feature)]
Quality:
Cross references:
Orphanet:2640 "Frontal bossing/prominent forehead" [Orphanet:2640]
OMIM: "Bulging forehead" [OMIM:Bulging forehead]
OMIM: "Prominent forehead" [OMIM:Prominent forehead]
OMIM: "Bulging forehead (rare)" [OMIM:Bulging forehead (rare)]
OMIM: "Forehead prominent" [OMIM:Forehead prominent]
OMIM: "Prominent forehead (homozygote)" [OMIM:Prominent forehead (homozygote)]
OMIM: "Prominent forehead (in some patients)" [OMIM:Prominent forehead (in some patients)]
OMIM: "Prominent forehead (major feature)" [OMIM:Prominent forehead (major feature)]
Is a (Direct Parents):
Orphanet Frontal bossing
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)
                   Prominent forehead(HPO:0011220)
MedDRA:
Database Frequency: 137 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3C syndrome (Orphanet:7)
AICA-ribosiduria (Orphanet:250977)
ALDH18A1-related De Barsy syndrome (Orphanet:35664)
AREDYLD syndrome (Orphanet:1133)
Acrocallosal syndrome (Orphanet:36)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Adenylosuccinate lyase deficiency (Orphanet:46)
Alpha-mannosidosis (Orphanet:61)
Atkin-Flaitz syndrome (Orphanet:1193)
Atypical Rett syndrome (Orphanet:3095)
Autosomal dominant Kenny-Caffey syndrome (Orphanet:93325)
Autosomal dominant Larsen syndrome (Orphanet:503)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive cutis laxa type 2B (Orphanet:357064)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
Bartter syndrome (Orphanet:112)
Bohring-Opitz syndrome (Orphanet:97297)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CLARK-BARAITSER SYNDROME (OMIM:300602)
CORPUS CALLOSUM, AGENESIS OF (OMIM:217990)
CRANIOMETADIAPHYSEAL DYSPLASIA (OMIM:269300)
CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS (OMIM:608279)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB (OMIM:614437)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Cenani-Lenz syndrome (Orphanet:3258)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Cortical blindness - intellectual deficit - polydactyly (Orphanet:1389)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Craniometadiaphyseal dysplasia, wormian bone type (Orphanet:85184)
D-2-@HYDROXYGLUTARIC ACIDURIA 1 (OMIM:600721)
D-2-hydroxyglutaric aciduria (Orphanet:79315)
De Barsy syndrome (Orphanet:2962)
Distal monosomy 1q (Orphanet:36367)
Dysosteosclerosis (Orphanet:1782)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2 (OMIM:615349)
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY (OMIM:614520)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 (OMIM:300672)
FG SYNDROME 4 (OMIM:300422)
Familial lambdoid synostosis (Orphanet:3267)
Frank-Ter Haar syndrome (Orphanet:137834)
Freeman-Sheldon syndrome (Orphanet:2053)
Fucosidosis (Orphanet:349)
GRANDDAD SYNDROME (OMIM:138920)
Goldblatt syndrome (Orphanet:166272)
HELSMOORTEL-VAN DER AA SYNDROME (OMIM:615873)
HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES (OMIM:236410)
Hurler syndrome (Orphanet:93473)
Hypertelorism, Teebi type (Orphanet:1519)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypotonia-speech impairment-severe cognitive delay syndrome (Orphanet:371364)
IMAGe syndrome (Orphanet:85173)
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES (OMIM:615966)
Infantile neuroaxonal dystrophy (Orphanet:35069)
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures (Orphanet:1568)
Intellectual deficit, X-linked - plagiocephaly (Orphanet:2898)
Intellectual deficit, X-linked, Armfield type (Orphanet:85276)
Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)
Keipert syndrome (Orphanet:2662)
Kenny-Caffey syndrome (Orphanet:2333)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Large congenital melanocytic nevus (Orphanet:626)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lymphedema - atrial septal defects - facial changes (Orphanet:86915)
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 (OMIM:615938)
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTICFEATURES (OMIM:613670)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 (OMIM:616158)
MENTAL RETARDATION, X-LINKED 19 (OMIM:300844)
MENTAL RETARDATION, X-LINKED 93 (OMIM:300659)
MENTAL RETARDATION, X-LINKED 99 (OMIM:300919)
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 (OMIM:300676)
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA (OMIM:608624)
MOVED TO 614732 (OMIM:300290)
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY (OMIM:601347)
Marshall-Smith syndrome (Orphanet:561)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Microcephalic osteodysplastic dysplasia, Saul-Wilson type (Orphanet:85172)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Microphthalmia with limb anomalies (Orphanet:1106)
Mowat-Wilson syndrome (Orphanet:2152)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Mulibrey nanism (Orphanet:2576)
Multiple sulfatase deficiency (Orphanet:585)
NOONAN SYNDROME 7 (OMIM:613706)
Neurofaciodigitorenal syndrome (Orphanet:2673)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
OSTEOGENESIS IMPERFECTA, TYPE XII (OMIM:613849)
OTOFACIOOSSEOUS-GONADAL SYNDROME (OMIM:601976)
Opitz G/BBB syndrome (Orphanet:2745)
Osteocraniostenosis (Orphanet:2763)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS (OMIM:600399)
PELGER-HUET ANOMALY (OMIM:169400)
PEROXISOME BIOGENESIS DISORDER 2B (OMIM:202370)
PGM1-CDG (Orphanet:319646)
PITUITARY HORMONE DEFICIENCY, COMBINED, 1 (OMIM:613038)
PMM2-CDG (Orphanet:79318)
PYCR1-related DeBarsy syndrome (Orphanet:293633)
Peters-plus syndrome (Orphanet:709)
Prolidase deficiency (Orphanet:742)
Rabson-Mendenhall syndrome (Orphanet:769)
Rudiger syndrome (Orphanet:3118)
SHORT RIB-POLYDACTYLY SYNDROME, TYPE III (OMIM:263510)
SHORT syndrome (Orphanet:3163)
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE (OMIM:613320)
STEEL SYNDROME (OMIM:615155)
Sanfilippo syndrome type D (Orphanet:79272)
Sanjad-Sakati syndrome (Orphanet:2323)
Schinzel-Giedion syndrome (Orphanet:798)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Sialuria (Orphanet:3166)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Syndromic diarrhea (Orphanet:84064)
TEMPLE SYNDROME (OMIM:616222)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
TRICHOHEPATOENTERIC SYNDROME 2 (OMIM:614602)
Tetrasomy 12p (Orphanet:884)
Ulnar/fibula ray defect - brachydactyly (Orphanet:52056)
WEBB-DATTANI SYNDROME (OMIM:615926)
X-linked Opitz G/BBB syndrome (Orphanet:306597)
X-linked intellectual deficit - cerebellar hypoplasia (Orphanet:137831)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
Zechi-Ceide syndrome (Orphanet:217017)
Zunich-Kaye syndrome (Orphanet:3474)