Abnormality of the rib cage
Symptom Information:
| Symptom ID: | HPO:0001547 | ||
| Synonyms: |
|
||
| Quality: | |||
| Cross references: |
|
||
| Is a (Direct Parents): |
|
||
| 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) MedDRA: |
||
| Database Frequency: | 25 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Adams-Oliver syndrome | (Orphanet:974) |
| Allan-Herndon-Dudley syndrome | (Orphanet:59) |
| Alpha-mannosidosis | (Orphanet:61) |
| Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
| Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
| Classic multiminicore myopathy | (Orphanet:324604) |
| Constriction rings syndrome | (Orphanet:295000) |
| Craniofrontonasal dysplasia | (Orphanet:1520) |
| Distal monosomy 10q | (Orphanet:96148) |
| Gordon syndrome | (Orphanet:376) |
| Growth delay due to insulin-like growth factor I resistance | (Orphanet:73273) |
| LUJAN-FRYNS SYNDROME | (OMIM:309520) |
| Lateral meningocele syndrome | (Orphanet:2789) |
| Lipodystrophy - intellectual deficit - deafness | (Orphanet:50811) |
| MGAT2-CDG | (Orphanet:79329) |
| MUCOLIPIDOSIS III GAMMA | (OMIM:252605) |
| Mowat-Wilson syndrome | (Orphanet:2152) |
| Mucolipidosis type 2 | (Orphanet:576) |
| NEMALINE MYOPATHY 2 | (OMIM:256030) |
| NEMALINE MYOPATHY 5 | (OMIM:605355) |
| Partial androgen insensitivity syndrome | (Orphanet:90797) |
| Renpenning syndrome | (Orphanet:3242) |
| Short stature - craniofacial anomalies - genital hypoplasia | (Orphanet:2994) |
| Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
| Spondylometaphyseal dysplasia, Kozlowski type | (Orphanet:93314) |