Pectus carinatum

Symptom Information:

Symptom ID: HPO:0000768
Synonyms:
Pectus carinatum (disorder) [Orphanet:15640]
Congenital pectus carinatum (disorder) [Orphanet:15640]
Pectus carinatum [Orphanet:15640]
Congenital pectus carinatum [Orphanet:15640]
Pectus carinatum [OMIM:Pectus carinatum]
Pectus carinatum [MedDRA:10034203]
Chicken breast [MedDRA:10034203]
Keeled breast [MedDRA:10034203]
Keeled chest [MedDRA:10034203]
Pectus galliatum [MedDRA:10034203]
Pigeon chest [MedDRA:10034203]
Pigeon-chested [MedDRA:10034203]
Pectus carinatum (in some patients) [OMIM:Pectus carinatum (in some patients)]
Pectus carinatum (in some) [OMIM:Pectus carinatum (in some)]
Pectus carinatum (superiorly) [OMIM:Pectus carinatum (superiorly)]
Quality:
Cross references:
HPO:0000917 "Superior pectus carinatum" [Orphanet:15640]
Orphanet:15640 "Pectus carinatum" [Orphanet:15640]
OMIM: "Pectus carinatum" [OMIM:Pectus carinatum]
OMIM: "Pectus carinatum (in some patients)" [OMIM:Pectus carinatum (in some patients)]
OMIM: "Pectus carinatum (in some)" [OMIM:Pectus carinatum (in some)]
OMIM: "Pectus carinatum (superiorly)" [OMIM:Pectus carinatum (superiorly)]
UMLS:C2939416 "Pectus carinatum" [Orphanet:15640]
UMLS:C0158731 "Congenital pectus carinatum" [Orphanet:15640]
Is a (Direct Parents):
Orphanet Abnormality of the sternum
MedDRA Thoracic musculoskeletal disorders
HPO         Abnormality of the sternum
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)