Broad ribs

Symptom Information:

Symptom ID: HPO:0000885
Synonyms:
Wide ribs [HPO:0000885]
Broad ribs [OMIM:Broad ribs]
Wide ribs [OMIM:Wide ribs]
Quality:
Cross references:
OMIM: "Broad ribs" [OMIM:Broad ribs]
OMIM: "Wide ribs" [OMIM:Wide ribs]
Is a (Direct Parents):
HPO         Abnormality of the ribs
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the thorax(HPO:0000765)
                   Abnormality of the rib cage(HPO:0001547)
                      Abnormality of the ribs(HPO:0000772)
                         Broad ribs(HPO:0000885)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

CRANIOMETADIAPHYSEAL DYSPLASIA (OMIM:269300)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Craniometadiaphyseal dysplasia, wormian bone type (Orphanet:85184)
Dysosteosclerosis (Orphanet:1782)
Fryns syndrome (Orphanet:2059)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Hurler-Scheie syndrome (Orphanet:93476)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal Kniest-like dysplasia (Orphanet:2347)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 6 (Orphanet:583)
Myhre syndrome (Orphanet:2588)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
Occipital horn syndrome (Orphanet:198)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Phocomelia, Schinzel type (Orphanet:2879)
RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA (OMIM:610319)
Schinzel-Giedion syndrome (Orphanet:798)
Sclerosteosis (Orphanet:3152)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
Weill-Marchesani syndrome (Orphanet:3449)