Thoracic hypoplasia

Symptom Information:

Symptom ID: HPO:0005257
Synonyms:
Small chest [HPO:0005257]
Small thorax [HPO:0005257]
Short rib cage [Orphanet:15200]
Short rib (finding) [Orphanet:15200]
Short thorax (finding) [Orphanet:15200]
Short rib [Orphanet:15200]
Short thorax [Orphanet:15200]
Small chest [OMIM:Small chest]
Small thorax [OMIM:Small thorax]
Thoracic hypoplasia [OMIM:Thoracic hypoplasia]
Short rib cage/thorax [Orphanet:15200]
Short ribs (in some patients) [OMIM:Short ribs (in some patients)]
Quality:
Cross references:
HPO:0010306 "Short thorax" [Orphanet:15200]
HPO:0000773 "Short ribs" [Orphanet:15200]
HPO:0000888 "Short, horizontal ribs" [Orphanet:15200]
Orphanet:15200 "Short rib cage/thorax" [Orphanet:15200]
OMIM: "Small chest" [OMIM:Small chest]
OMIM: "Small thorax" [OMIM:Small thorax]
OMIM: "Thoracic hypoplasia" [OMIM:Thoracic hypoplasia]
OMIM: "Short ribs (in some patients)" [OMIM:Short ribs (in some patients)]
UMLS:C0426817 "Short rib" [Orphanet:15200]
UMLS:C0426789 "Short thorax" [Orphanet:15200]
Is a (Direct Parents):
Orphanet Abnormality of the thorax
HPO         Abnormality of the thorax
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)
                   Thoracic hypoplasia(HPO:0005257)
MedDRA:
Database Frequency: 79 / 7739
Resource:

All diseases associated with this symptom:

3M syndrome (Orphanet:2616)
Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 1B (Orphanet:93298)
Achondrogenesis type 2 (Orphanet:93296)
Acrocapitofemoral dysplasia (Orphanet:63446)
Atelosteogenesis type II (Orphanet:56304)
Autosomal dominant brachyolmia (Orphanet:93304)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
BARATELA-SCOTT SYNDROME (OMIM:300881)
Bifunctional enzyme deficiency (Orphanet:300)
Bohring-Opitz syndrome (Orphanet:97297)
Brachyolmia (Orphanet:1293)
Brachyolmia type 1, Hobaek type (Orphanet:93301)
Brachyolmia type 1, Toledo type (Orphanet:93303)
Brachyolmia, Maroteaux type (Orphanet:93302)
Campomelic dysplasia (Orphanet:140)
Cartilage-hair hypoplasia (Orphanet:175)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Deafness - epiphyseal dysplasia - short stature (Orphanet:3218)
Diaphanospondylodysostosis (Orphanet:66637)
Disorder of sex development - intellectual deficit (Orphanet:2983)
Distal monosomy 17q (Orphanet:1597)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
Ellis Van Creveld syndrome (Orphanet:289)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
FIBROCHONDROGENESIS 1 (OMIM:228520)
FIBROCHONDROGENESIS 2 (OMIM:614524)
Fetal Gaucher disease (Orphanet:85212)
Fetal akinesia deformation sequence (Orphanet:994)
Fibrochondrogenesis (Orphanet:2021)
Fryns syndrome (Orphanet:2059)
Fukuda-Miyanomae-Nakata syndrome (Orphanet:2060)
HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES (OMIM:613124)
Jeune syndrome (Orphanet:474)
Kniest dysplasia (Orphanet:485)
Kyphomelic dysplasia (Orphanet:1801)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Marden-Walker syndrome (Orphanet:2461)
Microspherophakia - metaphyseal dysplasia (Orphanet:2551)
Mucopolysaccharidosis type 4 (Orphanet:582)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Otopalatodigital syndrome (Orphanet:669)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
Pyknoachondrogenesis (Orphanet:3003)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Saldino-Mainzer syndrome (Orphanet:140969)
Short rib-polydactyly syndrome (Orphanet:1505)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)
Short-rib thoracic dysplasia 3 with or without polydactyly (OMIM:613091)
Shwachman-Diamond syndrome (Orphanet:811)
Sialidosis type 1 (Orphanet:812)
Sialidosis type 2 (Orphanet:87876)
Sialuria (Orphanet:3166)
Spondylo-ocular syndrome (Orphanet:85194)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification (Orphanet:93358)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondyloepimetaphyseal dysplasia, matrilin-3 type (Orphanet:156728)
Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia (Orphanet:253)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondyloepiphyseal dysplasia tarda (Orphanet:93284)
Spondyloepiphyseal dysplasia, Cantu type (Orphanet:163654)
Spondyloepiphyseal dysplasia, Kimberley type (Orphanet:93283)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Thanatophoric dysplasia (Orphanet:2655)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Thanatophoric dysplasia type 2 (Orphanet:93274)
Trisomy 1q (Orphanet:261344)
Wolcott-Rallison syndrome (Orphanet:1667)