Prominent forehead
Symptom Information:
Symptom ID: | HPO:0011220 | |||||||||
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) Prominent forehead(HPO:0011220) MedDRA: |
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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) |