Sloping forehead

Symptom Information:

Symptom ID: HPO:0000340
Synonyms:
Receding forehead [HPO:0000340]
Receding forehead [OMIM:Receding forehead]
Sloping forehead [OMIM:Sloping forehead]
Sloping forehead [Orphanet:2720]
Sloping forehead (in some patients) [OMIM:Sloping forehead (in some patients)]
Quality:
Cross references:
Orphanet:2720 "Sloping forehead" [Orphanet:2720]
OMIM: "Receding forehead" [OMIM:Receding forehead]
OMIM: "Sloping forehead" [OMIM:Sloping forehead]
OMIM: "Sloping forehead (in some patients)" [OMIM:Sloping forehead (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the forehead
Orphanet Abnormality of the skull
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:
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)