Prominent supraorbital ridges
Symptom Information:
Symptom ID: | HPO:0000336 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) |