Abnormality of the ribs

Symptom Information:

Symptom ID: HPO:0000772
Rib abnormalities [HPO:0000772]
Rib anomalies [HPO:0000772]
Rib anomaly [Orphanet:15720]
Rib abnormalities [OMIM:Rib abnormalities]
Rib anomalies [OMIM:Rib anomalies]
Anomalies of the ribs [Orphanet:15720]
Rib abnormalities (55%) [OMIM:Rib abnormalities (55%)]
Cross references:
Orphanet:15720 "Anomalies of the ribs" [Orphanet:15720]
OMIM: "Rib abnormalities" [OMIM:Rib abnormalities]
OMIM: "Rib anomalies" [OMIM:Rib anomalies]
OMIM: "Rib abnormalities (55%)" [OMIM:Rib abnormalities (55%)]
Is a (Direct Parents):
HPO         Abnormality of the rib cage
HPO         Rib gap
HPO         Calcification of ribs
Orphanet Abnormality of the thorax
Is a (Whole tree): HPO:
    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)
Database Frequency: 146 / 7739

All diseases associated with this symptom:

10q22.3q23.3 microduplication syndrome (Orphanet:276422)
1p36 deletion syndrome (Orphanet:1606)
3M syndrome (Orphanet:2616)
Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 1B (Orphanet:93298)
Achondroplasia (Orphanet:15)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acro-renal-mandibular syndrome (Orphanet:958)
Adamantinoma (Orphanet:55881)
Alagille syndrome (Orphanet:52)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Antley-Bixler syndrome (Orphanet:83)
Autosomal dominant osteosclerosis, Worth type (Orphanet:2790)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
BRESEK syndrome (Orphanet:85284)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
Brachyolmia type 1, Toledo type (Orphanet:93303)
Braddock syndrome (Orphanet:52047)
CHARGE syndrome (Orphanet:138)
CHILD syndrome (Orphanet:139)
Cartilage-hair hypoplasia (Orphanet:175)
Cat-eye syndrome (Orphanet:195)
Catel-Manzke syndrome (Orphanet:1388)
Caudal appendage - deafness (Orphanet:1123)
Cenani-Lenz syndrome (Orphanet:3258)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Cleidocranial dysplasia (Orphanet:1452)
Cloverleaf skull - multiple congenital anomalies (Orphanet:93267)
Cole-Carpenter syndrome (Orphanet:2050)
Congenital osteogenesis imperfecta - microcephaly - cataracts (Orphanet:2772)
Cooper-Jabs syndrome (Orphanet:1488)
Craniodiaphyseal dysplasia (Orphanet:1513)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Desmosterolosis (Orphanet:35107)
Diastrophic dwarfism (Orphanet:628)
Ear-patella-short stature syndrome (Orphanet:2554)
Familial osteodysplasia, Anderson type (Orphanet:2769)
Femoral-facial syndrome (Orphanet:1988)
Fibrochondrogenesis (Orphanet:2021)
Focal dermal hypoplasia (Orphanet:2092)
Goldenhar syndrome (Orphanet:374)
Gorlin syndrome (Orphanet:377)
Grant syndrome (Orphanet:2097)
Greenberg dysplasia (Orphanet:1426)
Grix-Blankenship-Peterson syndrome (Orphanet:2099)
Hallermann-Streiff syndrome (Orphanet:2108)
Heart defects - limb shortening (Orphanet:1354)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Holt-Oram syndrome (Orphanet:392)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypophosphatasia (Orphanet:436)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Imperforate oropharynx - costo vetebral anomalies (Orphanet:2759)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Intellectual deficit, X-linked, Kroes type (Orphanet:163961)
Intestinal lymphangiectasia (Orphanet:36204)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Isolated spina bifida (Orphanet:823)
Jeune syndrome (Orphanet:474)
KBG syndrome (Orphanet:2332)
Kindler syndrome (Orphanet:2908)
Kyphomelic dysplasia (Orphanet:1801)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia (Orphanet:2005)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
Lethal recessive chondrodysplasia (Orphanet:1423)
MURCS association (Orphanet:2578)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Metatropic dysplasia (Orphanet:2635)
Microcephaly - cervical spine fusion anomalies (Orphanet:2522)
Microcephaly - seizures - intellectual deficit - heart disease (Orphanet:2519)
Monosomy 9p (Orphanet:261112)
Mosaic trisomy 14 (Orphanet:1703)
Mosaic trisomy 8 (Orphanet:96061)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mucopolysaccharidosis type 6 (Orphanet:583)
Myhre syndrome (Orphanet:2588)
Nestor-Guillermo progeria syndrome (Orphanet:280576)
Neurogenic thoracic outlet syndrome (Orphanet:100073)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Oculocerebrorenal syndrome (Orphanet:534)
Osteocraniostenosis (Orphanet:2763)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Osteogenesis imperfecta (Orphanet:666)
Osteopetrosis (Orphanet:2781)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
PAGOD syndrome (Orphanet:991)
PHAVER syndrome (Orphanet:2876)
Parastremmatic dwarfism (Orphanet:2646)
Pelvis-shoulder dysplasia (Orphanet:2839)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Pilotto syndrome (Orphanet:2894)
Poland syndrome (Orphanet:2911)
Prune belly syndrome (Orphanet:2970)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Pyle disease (Orphanet:3005)
Radio-renal syndrome (Orphanet:3015)
Scheie syndrome (Orphanet:93474)
Schinzel-Giedion syndrome (Orphanet:798)
Schwartz-Jampel syndrome (Orphanet:800)
Short rib-polydactyly syndrome (Orphanet:1505)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
TMCO1 defect syndrome (Orphanet:228407)
Thin ribs - tubular bones - dysmorphism (Orphanet:1506)
Thoracic outlet syndrome (Orphanet:97330)
Thoracolaryngopelvic dysplasia (Orphanet:3317)
Thoracomelic dysplasia (Orphanet:1803)
Townes-Brocks syndrome (Orphanet:857)
Trisomy 13 (Orphanet:3378)
Trisomy 18 (Orphanet:3380)
Ulbright-Hodes syndrome (Orphanet:3404)
VACTERL/VATER association (Orphanet:887)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Van den Ende-Gupta syndrome (Orphanet:2460)
X-linked dominant chondrodysplasia, Chassaing-Lacombe type (Orphanet:163966)
Zimmermann-Laband syndrome (Orphanet:3473)