Prominent supraorbital ridges

Symptom Information:

Symptom ID: HPO:0000336
Synonyms:
Prominent supraorbital ridge [HPO:0000336]
Prominent supraorbital ridge [OMIM:Prominent supraorbital ridge]
Prominent supraorbital ridges [OMIM:Prominent supraorbital ridges]
Prominent supraorbital ridge [Orphanet:3400]
Quality:
Cross references:
Orphanet:3400 "Prominent supraorbital ridge" [Orphanet:3400]
OMIM: "Prominent supraorbital ridge" [OMIM:Prominent supraorbital ridge]
OMIM: "Prominent supraorbital ridges" [OMIM:Prominent supraorbital ridges]
Is a (Direct Parents):
Orphanet Abnormal facial shape
HPO         Abnormality of the supraorbital ridges
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 orbital region(HPO:0000315)
                   Abnormality of the supraorbital ridges(HPO:0100538)
                      Prominent supraorbital ridges(HPO:0000336)
MedDRA:
Database Frequency: 45 / 7739
Resource:

All diseases associated with this symptom:

AXENFELD-RIEGER SYNDROME, TYPE 1 (OMIM:180500)
Alpha-mannosidosis (Orphanet:61)
Atkin-Flaitz syndrome (Orphanet:1193)
Axenfeld-Rieger syndrome (Orphanet:782)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
CUTIS VERTICIS GYRATA, RETINITIS PIGMENTOSA, AND SENSORINEURAL DEAFNESS (OMIM:605685)
Coffin-Lowry syndrome (Orphanet:192)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniosynostosis - intracranial calcifications (Orphanet:52054)
Fabry disease (Orphanet:324)
Frontometaphyseal dysplasia (Orphanet:1826)
GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY (OMIM:608278)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Hennekam-Beemer syndrome (Orphanet:2135)
Hurler syndrome (Orphanet:93473)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Intellectual deficit, X-linked - hypogammaglobulinemia - progressive neurological deterioration (Orphanet:85317)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
Intellectual deficit, X-linked, Shashi type (Orphanet:85286)
Isolated trigonocephaly (Orphanet:3366)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45 (OMIM:615979)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
McDonough syndrome (Orphanet:2471)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Microbrachycephaly - ptosis - cleft lip (Orphanet:2511)
Monosomy 22q13 (Orphanet:48652)
Monosomy 5p (Orphanet:281)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
OSTEOGENESIS IMPERFECTA, TYPE XII (OMIM:613849)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otopalatodigital syndrome type 2 (Orphanet:90652)
PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS (OMIM:600399)
Pectus excavatum - macrocephaly - dysplastic nails (Orphanet:2835)
Pyle disease (Orphanet:3005)
SHORT syndrome (Orphanet:3163)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Wilson-Turner syndrome (Orphanet:3459)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
X-linked intellectual deficit - cerebellar hypoplasia (Orphanet:137831)
X-linked intellectual disability due to GRIA3 anomalies (Orphanet:364028)