Pectus carinatum
Symptom Information:
Symptom ID: | HPO:0000768 | |||||||||||||||
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 sternum(HPO:0000766) Pectus carinatum(HPO:0000768) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Thoracic disorders (excl lung and pleura)(MedDRA:10013369) Thoracic musculoskeletal disorders(MedDRA:10043475) Pectus carinatum(HPO:0000768) |
|||||||||||||||
Database Frequency: | 136 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
20p12.3 microdeletion syndrome | (Orphanet:261295) |
3q29 microdeletion syndrome | (Orphanet:65286) |
AORTIC ANEURYSM, FAMILIAL THORACIC 9 | (OMIM:616166) |
Acro-pectoral syndrome | (Orphanet:85203) |
Acro-pectoro-renal dysplasia | (Orphanet:956) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Acrocapitofemoral dysplasia | (Orphanet:63446) |
Acroosteolysis, dominant type | (Orphanet:955) |
Alpha-mannosidosis | (Orphanet:61) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Aspartylglucosaminuria | (Orphanet:93) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Autosomal recessive spastic paraplegia type 53 | (Orphanet:319199) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
BRUCK SYNDROME 1 | (OMIM:259450) |
BRUCK SYNDROME 2 | (OMIM:609220) |
Becker nevus syndrome | (Orphanet:64755) |
Brachyolmia type 1, Hobaek type | (Orphanet:93301) |
Bruck syndrome | (Orphanet:2771) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CATEL-MANZKE SYNDROME | (OMIM:616145) |
CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS | (OMIM:608279) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Catel-Manzke syndrome | (Orphanet:1388) |
Classical homocystinuria | (Orphanet:394) |
Coffin-Lowry syndrome | (Orphanet:192) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
Costello syndrome | (Orphanet:3071) |
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
Cryptorchidism - arachnodactyly - intellectual deficit | (Orphanet:1548) |
Cutis laxa | (Orphanet:209) |
DESBUQUOIS DYSPLASIA 2 | (OMIM:615777) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Dysmorphism - pectus carinatum - joint laxity | (Orphanet:2104) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Generalized resistance to thyroid hormone | (Orphanet:3221) |
Geroderma osteodysplastica | (Orphanet:2078) |
Goldblatt syndrome | (Orphanet:166272) |
HUNTER-MACDONALD SYNDROME | (OMIM:611962) |
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES | (OMIM:614684) |
Hirsutism - skeletal dysplasia - intellectual deficit | (Orphanet:2156) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypospadias - hypertelorism - coloboma and deafness | (Orphanet:157788) |
Hypotonia-speech impairment-severe cognitive delay syndrome | (Orphanet:371364) |
Intellectual deficit - hypotonia - skin hyperpigmentation | (Orphanet:3050) |
Intellectual deficit - myopathy - short stature - endocrine defect | (Orphanet:3068) |
Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked, Raymond type | (Orphanet:163953) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Juvenile Paget disease | (Orphanet:2801) |
KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS | (OMIM:245160) |
LEOPARD SYNDROME 1 | (OMIM:151100) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
MARFANOID HYPERMOBILITY SYNDROME | (OMIM:154750) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 | (OMIM:300676) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
MUCOLIPIDOSIS III GAMMA | (OMIM:252605) |
Marden-Walker syndrome | (Orphanet:2461) |
Marfan syndrome type 1 | (Orphanet:284963) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
McDonough syndrome | (Orphanet:2471) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
Mucopolysaccharidosis type 4 | (Orphanet:582) |
Mucopolysaccharidosis type 7 | (Orphanet:584) |
Multiple epiphyseal dysplasia, Al-Gazali type | (Orphanet:166024) |
NEMALINE MYOPATHY 5 | (OMIM:605355) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
OSTEOGENESIS IMPERFECTA, TYPE IX | (OMIM:259440) |
OSTEOGENESIS IMPERFECTA, TYPE XII | (OMIM:613849) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
Occipital horn syndrome | (Orphanet:198) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Osteogenesis imperfecta | (Orphanet:666) |
Parana hard-skin syndrome | (Orphanet:2812) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Parastremmatic dwarfism | (Orphanet:2646) |
Penoscrotal transposition | (Orphanet:2842) |
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis | (Orphanet:65288) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Prune belly syndrome | (Orphanet:2970) |
RIENHOFF SYNDROME | (OMIM:615582) |
Richieri Costa-da Silva syndrome | (Orphanet:3101) |
Ruvalcaba syndrome | (Orphanet:3121) |
SCARF syndrome | (Orphanet:3134) |
SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS | (OMIM:609654) |
SMITH-MCCORT DYSPLASIA 2 | (OMIM:615222) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT | (OMIM:184100) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE | (OMIM:609223) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Sialidosis type 1 | (Orphanet:812) |
Sialidosis type 2 | (Orphanet:87876) |
Spondyloepimetaphyseal dysplasia congenita, Strudwick type | (Orphanet:93346) |
Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
Spondyloepiphyseal dysplasia congenita | (Orphanet:94068) |
Spondyloepiphyseal dysplasia tarda | (Orphanet:93284) |
Spondylometaphyseal dysplasia, A4 type | (Orphanet:168555) |
Spondylometaphyseal dysplasia, Golden type | (Orphanet:168544) |
Spondylometaphyseal dysplasia, Kozlowski type | (Orphanet:93314) |
Spondyloperipheral dysplasia - short ulna | (Orphanet:1856) |
Stickler syndrome | (Orphanet:828) |
Stickler syndrome type 3 | (Orphanet:166100) |
Symptomatic form of Coffin-Lowry syndrome in female carriers | (Orphanet:276630) |
Synostosis - microcephaly - scoliosis | (Orphanet:3268) |
TMCO1 defect syndrome | (Orphanet:228407) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Ulnar-mammary syndrome | (Orphanet:3138) |
X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
X-linked spondyloepimetaphyseal dysplasia | (Orphanet:93349) |