Thoracic dysplasia

Symptom Information:

Symptom ID: HPO:0006644
Synonyms:
Dysplasia [HPO:0006644]
Thoracic dysplasia [OMIM:Thoracic dysplasia]
Dysplasia [OMIM:Dysplasia]
Dysplasia [MedDRA:10058314]
Quality:
Cross references:
OMIM: "Thoracic dysplasia" [OMIM:Thoracic dysplasia]
OMIM: "Dysplasia" [OMIM:Dysplasia]
UMLS:C0334044 "Dysplasia" [HPO:0006644]
Is a (Direct Parents):
HPO         Abnormality of the rib cage
MedDRA Trophic disorders
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)
                      Thoracic dysplasia(HPO:0006644)
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    Tissue disorders NEC(MedDRA:10007867)
       Trophic disorders(MedDRA:10044694)
          Thoracic dysplasia(HPO:0006644)
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Bone dysplasia, lethal Holmgren type (Orphanet:1842)
CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA (OMIM:211930)
Heart defects - limb shortening (Orphanet:1354)
Jeune syndrome (Orphanet:474)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)
Short-rib thoracic dysplasia 11 with or without polydactyly (OMIM:615633)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
Short-rib thoracic dysplasia 7 with or without polydactyly (OMIM:614091)
Short-rib thoracic dysplasia 8 with or without polydactyly (OMIM:615503)
Thoracic dysplasia-hydrocephalus syndrome (Orphanet:1861)