Thin ribs
Symptom Information:
Symptom ID: | HPO:0000883 | ||||
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) Thin ribs(HPO:0000883) MedDRA: |
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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) |