Abnormality of the ribs
Symptom Information:
Symptom ID: | HPO:0000772 | ||||||||
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) MedDRA: |
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Database Frequency: | 146 / 7739 | ||||||||
Resource: |
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) |
PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES | (OMIM:602196) |
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) |
SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE | (OMIM:277300) |
SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE | (OMIM:613686) |
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) |