High forehead
Symptom Information:
Symptom ID: | HPO:0000348 | |||||||
Synonyms: |
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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) High forehead(HPO:0000348) MedDRA: |
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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) |