Sloping forehead
Symptom Information:
Symptom ID: | HPO:0000340 | |||||
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) Sloping forehead(HPO:0000340) MedDRA: |
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Database Frequency: | 86 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
3-hydroxyisobutyric aciduria | (Orphanet:939) |
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 | (OMIM:613404) |
ASPARAGINE SYNTHETASE DEFICIENCY | (OMIM:615574) |
Acrocallosal syndrome | (Orphanet:36) |
Acrocraniofacial dysostosis | (Orphanet:949) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Amish lethal microcephaly | (Orphanet:99742) |
Anonychia - microcephaly | (Orphanet:1094) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Autosomal dominant microcephaly | (Orphanet:2514) |
Autosomal recessive chorioretinopathy-microcephaly | (Orphanet:2518) |
Bangstad syndrome | (Orphanet:1227) |
Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
Bowen-Conradi syndrome | (Orphanet:1270) |
CEREBROOCULOFACIOSKELETAL SYNDROME 1 | (OMIM:214150) |
CLN10 disease | (Orphanet:228337) |
COFS syndrome | (Orphanet:1466) |
CUTIS VERTICIS GYRATA, RETINITIS PIGMENTOSA, AND SENSORINEURAL DEAFNESS | (OMIM:605685) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Cernunnos-XLF deficiency | (Orphanet:169079) |
Cleidocranial dysplasia | (Orphanet:1452) |
Congenital intrauterine infection-like syndrome | (Orphanet:1229) |
Congenital neuronal ceroid lipofuscinosis | (Orphanet:168486) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA | (OMIM:221950) |
Distal trisomy 15q | (Orphanet:1707) |
Dubowitz syndrome | (Orphanet:235) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Fanconi anemia | (Orphanet:84) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS | (OMIM:610680) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, Wolff type | (Orphanet:3080) |
Intellectual deficit, X-linked, Abidi type | (Orphanet:85273) |
Keutel syndrome | (Orphanet:85202) |
LISSENCEPHALY 6 WITH MICROCEPHALY | (OMIM:616212) |
Lathosterolosis | (Orphanet:46059) |
Lissencephaly syndrome, Norman-Roberts type | (Orphanet:89844) |
MEHMO syndrome | (Orphanet:85282) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39 | (OMIM:615541) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:616080) |
MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:616051) |
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS | (OMIM:604317) |
MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:604804) |
MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:608716) |
MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:614673) |
MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2 | (OMIM:616171) |
MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLARATROPHY | (OMIM:615760) |
MICROHYDRANENCEPHALY | (OMIM:605013) |
Macular coloboma - cleft palate - hallux valgus | (Orphanet:91494) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Meckel syndrome, type 12 | (OMIM:616258) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Microcephalic primordial dwarfism due to ZNF335 deficiency | (Orphanet:329228) |
Microcephaly - cervical spine fusion anomalies | (Orphanet:2522) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Microcephaly-cardiomyopathy syndrome | (Orphanet:2515) |
Morse-Rawnsley-Sargent syndrome | (Orphanet:2570) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
NEU-LAXOVA SYNDROME 2 | (OMIM:616038) |
Neu-Laxova syndrome | (Orphanet:2671) |
Nijmegen breakage syndrome | (Orphanet:647) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2B | (OMIM:612389) |
Paraplegia - intellectual deficit - hyperkeratosis | (Orphanet:2824) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Premature chromosome condensation with microcephaly and intellectual deficit | (Orphanet:52183) |
Primordial short stature - microdontia - opalescent and rootless teeth | (Orphanet:46658) |
Ptosis - upper ocular movement limitation - absence of lacrimal punctum | (Orphanet:228396) |
Ring chromosome 8 | (Orphanet:1450) |
SECKEL SYNDROME 1 | (OMIM:210600) |
SECKEL SYNDROME 5 | (OMIM:613823) |
SHORT STATURE-OBESITY SYNDROME | (OMIM:269870) |
Say-Barber-Miller syndrome | (Orphanet:3132) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Seckel syndrome | (Orphanet:808) |
Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
Warsaw breakage syndrome | (Orphanet:280558) |
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 | (OMIM:208085) |