High forehead

Symptom Information:

Symptom ID: HPO:0000348
Synonyms:
High forehead [OMIM:High forehead]
High forehead [Orphanet:2680]
Forehead high [OMIM:Forehead high]
High forehead (1/4 patients) [OMIM:High forehead (1/4 patients)]
High forehead (in one family) [OMIM:High forehead (in one family)]
High forehead (rare) [OMIM:High forehead (rare)]
Tall forehead [IBIS,cm]
Quality:
Cross references:
Orphanet:2680 "High forehead" [Orphanet:2680]
OMIM: "High forehead" [OMIM:High forehead]
OMIM: "Forehead high" [OMIM:Forehead high]
OMIM: "High forehead (1/4 patients)" [OMIM:High forehead (1/4 patients)]
OMIM: "High forehead (in one family)" [OMIM:High forehead (in one family)]
OMIM: "High forehead (rare)" [OMIM:High forehead (rare)]
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)
                   High forehead(HPO:0000348)
MedDRA:
Database Frequency: 157 / 7739
Resource:

All diseases associated with this symptom:

14q22q23 microdeletion syndrome (Orphanet:264200)
15q24 microdeletion syndrome (Orphanet:94065)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
16q24.3 microdeletion syndrome (Orphanet:261250)
17p13.3 microduplication syndrome (Orphanet:217385)
17q12 microdeletion syndrome (Orphanet:261265)
19q13.11 microdeletion syndrome (Orphanet:217346)
1q44 microdeletion syndrome (Orphanet:238769)
22q11.2 microduplication syndrome (Orphanet:1727)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q32q33 microdeletion syndrome (Orphanet:251019)
3C syndrome (Orphanet:7)
3q29 microduplication (Orphanet:251038)
4q21 microdeletion syndrome (Orphanet:238750)
5q14.3 microdeletion syndrome (Orphanet:228384)
8p23.1 microdeletion syndrome (Orphanet:251071)
8q21.11 microdeletion syndrome (Orphanet:284160)
ALG11-CDG (Orphanet:280071)
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES (OMIM:300887)
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 (OMIM:170995)
Acro-cardio-facial syndrome (Orphanet:2008)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia (Orphanet:52055)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Apert syndrome (Orphanet:87)
Bifunctional enzyme deficiency (Orphanet:300)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
CAMPOMELIC DYSPLASIA (OMIM:114290)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION (OMIM:601088)
CHROMOSOME 16q22 DELETION SYNDROME (OMIM:614541)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
Campomelic dysplasia (Orphanet:140)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Chondrodysplasia with joint dislocations, gPAPP type (Orphanet:280586)
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis (Orphanet:171839)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Deaf blind hypopigmentation syndrome, Yemenite type (Orphanet:3214)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Developmental malformations - deafness - dystonia (Orphanet:79107)
Dubowitz syndrome (Orphanet:235)
Early infantile epileptic encephalopathy without suppression burst (Orphanet:369894)
Emery-Nelson syndrome (Orphanet:1927)
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria (Orphanet:1035)
Epimetaphyseal skeletal dysplasia (Orphanet:1819)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Fallot complex - intellectual deficit - growth delay (Orphanet:3304)
Familial intestinal malrotation - facial anomalies (Orphanet:2454)
Familial scaphocephaly syndrome, McGillivray type (Orphanet:168624)
Fine-Lubinsky syndrome (Orphanet:1272)
Flat face - microstomia - ear anomaly (Orphanet:1968)
GAPO syndrome (Orphanet:2067)
GIACHETI SYNDROME (OMIM:612917)
German syndrome (Orphanet:2077)
Greenberg dysplasia (Orphanet:1426)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hypertrichosis cubiti - short stature (Orphanet:2220)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit - hypoplastic corpus callosum - preauricular tag (Orphanet:1495)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Intellectual deficit, X-linked - hypotonia - facial dysmorphism - aggressive behavior (Orphanet:85329)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
Isolated cloverleaf skull syndrome (Orphanet:2343)
Isotretinoin-like syndrome (Orphanet:2306)
Jacobsen syndrome (Orphanet:2308)
Koolen-De Vries syndrome (Orphanet:96169)
Kyphomelic dysplasia (Orphanet:1801)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Laron syndrome (Orphanet:633)
Lethal recessive chondrodysplasia (Orphanet:1423)
Lymphedema - atrial septal defects - facial changes (Orphanet:86915)
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY (OMIM:606369)
MEDNIK syndrome (Orphanet:171851)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35 (OMIM:615162)
MOMO syndrome (Orphanet:2563)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
Macrocephaly - short stature - paraplegia (Orphanet:2427)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Metatropic dysplasia (Orphanet:2635)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mietens syndrome (Orphanet:2557)
Miller-Dieker syndrome (Orphanet:531)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mowat-Wilson syndrome (Orphanet:2152)
Mucolipidosis type 2 (Orphanet:576)
Mulibrey nanism (Orphanet:2576)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Neonatal adrenoleukodystrophy (Orphanet:44)
Non-distal trisomy 10q (Orphanet:1695)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
Occipital horn syndrome (Orphanet:198)
Oculodentodigital dysplasia (Orphanet:2710)
Odontotrichomelic syndrome (Orphanet:2723)
Osteosclerosis - developmental delay - craniosynostosis (Orphanet:178377)
PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER) (OMIM:614882)
PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER) (OMIM:614883)
PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) (OMIM:614887)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) (OMIM:214110)
PEROXISOME BIOGENESIS DISORDER 2B (OMIM:202370)
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) (OMIM:614866)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Paraplegia - intellectual deficit - hyperkeratosis (Orphanet:2824)
Parastremmatic dwarfism (Orphanet:2646)
Patent arterial duct (Orphanet:706)
Paternal 20q13.2q13.3 microdeletion syndrome (Orphanet:261304)
Perlman syndrome (Orphanet:2849)
Pfeiffer syndrome (Orphanet:710)
Pfeiffer syndrome type 1 (Orphanet:93258)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Pierre Robin syndrome - faciodigital anomaly (Orphanet:2888)
Potocki-Shaffer syndrome (Orphanet:52022)
Pycnodysostosis (Orphanet:763)
RAPP-HODGKIN SYNDROME (OMIM:129400)
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 (OMIM:616331)
Rhizomelic chondrodysplasia punctata type 2 (Orphanet:309796)
Ring chromosome 8 (Orphanet:1450)
Ruvalcaba syndrome (Orphanet:3121)
SECKEL SYNDROME 4 (OMIM:613676)
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES (OMIM:615789)
Saethre-Chotzen syndrome (Orphanet:794)
Sanjad-Sakati syndrome (Orphanet:2323)
Schinzel-Giedion syndrome (Orphanet:798)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Sotos syndrome (Orphanet:821)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Stormorken-Sjaastad-Langslet syndrome (Orphanet:3204)
Thomas syndrome (Orphanet:3316)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Thrombocytopenia - absent radius (Orphanet:3320)
Trisomy 18 (Orphanet:3380)
Trisomy 8q (Orphanet:1752)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Williams syndrome (Orphanet:904)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)
Zellweger syndrome (Orphanet:912)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)