Thin ribs

Symptom Information:

Symptom ID: HPO:0000883
Synonyms:
Slender ribs [HPO:0000883]
Thin rib [HPO:0000883]
Slender ribs [OMIM:Slender ribs]
Thin ribs [OMIM:Thin ribs]
Quality:
Cross references:
OMIM: "Slender ribs" [OMIM:Slender ribs]
OMIM: "Thin ribs" [OMIM:Thin 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)
                         Thin ribs(HPO:0000883)
MedDRA:
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

Acro-renal-mandibular syndrome (Orphanet:958)
Autosomal recessive Kenny-Caffey syndrome (Orphanet:93324)
CAMPOMELIC DYSPLASIA (OMIM:114290)
COLE-CARPENTER SYNDROME 2 (OMIM:616294)
Campomelic dysplasia (Orphanet:140)
Ear-patella-short stature syndrome (Orphanet:2554)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Fetal akinesia deformation sequence (Orphanet:994)
Fetal akinesia-cerebral and retinal hemorrhage syndrome (Orphanet:363409)
Fibrochondrogenesis (Orphanet:2021)
Fryns syndrome (Orphanet:2059)
Hallermann-Streiff syndrome (Orphanet:2108)
KAGAMI-OGATA SYNDROME (OMIM:608149)
Lethal multiple pterygium syndrome (Orphanet:33108)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
Marden-Walker syndrome (Orphanet:2461)
Mulibrey nanism (Orphanet:2576)
OSTEOGENESIS IMPERFECTA, TYPE VIII (OMIM:610915)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
OSTEOGENESIS IMPERFECTA, TYPE XV (OMIM:615220)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Spondyloepimetaphyseal dysplasia, Bieganski type (Orphanet:168448)
Stüve-Wiedemann syndrome (Orphanet:3206)
Suarez-Stickler syndrome (Orphanet:166277)
Ulbright-Hodes syndrome (Orphanet:3404)
Van den Ende-Gupta syndrome (Orphanet:2460)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
X-linked dominant chondrodysplasia, Chassaing-Lacombe type (Orphanet:163966)
X-linked lethal multiple pterygium syndrome (Orphanet:79447)