Shallow orbits

Symptom Information:

Symptom ID: HPO:0000586
Synonyms:
Small shallow orbits [HPO:0000586]
Underdeveloped supraorbital ridges [Orphanet:3420]
Shallow orbits [OMIM:Shallow orbits]
Small shallow orbits [OMIM:Small shallow orbits]
Flat supraorbital ridge [Orphanet:3420]
Flat supraorbital ridges [OMIM:Flat supraorbital ridges]
Quality:
Cross references:
HPO:0009891 "Hypoplasia of the supraorbital ridges" [Orphanet:3420]
Orphanet:3420 "Flat supraorbital ridge" [Orphanet:3420]
OMIM: "Shallow orbits" [OMIM:Shallow orbits]
OMIM: "Small shallow orbits" [OMIM:Small shallow orbits]
OMIM: "Flat supraorbital ridges" [OMIM:Flat supraorbital ridges]
Is a (Direct Parents):
HPO         Proptosis
Orphanet Abnormal facial shape
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 globe location(HPO:0100886)
                      Proptosis(HPO:0000520)
                         Shallow orbits(HPO:0000586)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of globe location(HPO:0100886)
                      Proptosis(HPO:0000520)
                         Shallow orbits(HPO:0000586)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of globe location(HPO:0100886)
                   Proptosis(HPO:0000520)
                      Shallow orbits(HPO:0000586)
MedDRA:
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

Apert syndrome (Orphanet:87)
Autosomal dominant Larsen syndrome (Orphanet:503)
Cole-Carpenter syndrome (Orphanet:2050)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Crouzon disease (Orphanet:207)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
Fine-Lubinsky syndrome (Orphanet:1272)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Hurler syndrome (Orphanet:93473)
Marshall-Smith syndrome (Orphanet:561)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
Osteoglophonic dwarfism (Orphanet:2645)
Pfeiffer syndrome (Orphanet:710)
ROBERTS SYNDROME (OMIM:268300)
ROBINOW-SORAUF SYNDROME (OMIM:180750)
Roberts syndrome (Orphanet:3103)
Saethre-Chotzen syndrome (Orphanet:794)
Sakati-Nyhan syndrome (Orphanet:3128)
Schinzel-Giedion syndrome (Orphanet:798)
Shprintzen-Goldberg syndrome (Orphanet:2462)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
Weill-Marchesani syndrome (Orphanet:3449)