Broad ribs
Symptom Information:
Symptom ID: | HPO:0000885 | |||
Synonyms: |
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Quality: | ||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |