Superior pectus carinatum

Symptom Information:

Symptom ID: HPO:0000917
Synonyms:
Pectus carinatum superiorly [HPO:0000917]
Pectus carinatum [Orphanet:15640]
Pectus carinatum (disorder) [Orphanet:15640]
Congenital pectus carinatum (disorder) [Orphanet:15640]
Congenital pectus carinatum [Orphanet:15640]
Pectus carinatum superiorly [OMIM:Pectus carinatum superiorly]
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:0000768 "Pectus carinatum" [Orphanet:15640]
Orphanet:15640 "Pectus carinatum" [Orphanet:15640]
OMIM: "Pectus carinatum superiorly" [OMIM:Pectus carinatum superiorly]
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):
HPO         Pectus carinatum
MedDRA Thoracic musculoskeletal disorders
Orphanet 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)
                         Superior pectus carinatum(HPO:0000917)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Thoracic disorders (excl lung and pleura)(MedDRA:10013369)
       Thoracic musculoskeletal disorders(MedDRA:10043475)
          Superior pectus carinatum(HPO:0000917)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Autosomal recessive spastic paraplegia type 53 (Orphanet:319199)
Fine-Lubinsky syndrome (Orphanet:1272)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Mowat-Wilson syndrome (Orphanet:2152)
NOONAN SYNDROME 1 (OMIM:163950)
Noonan syndrome (Orphanet:648)
OSTEOGENESIS IMPERFECTA, TYPE XIII (OMIM:614856)
SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS (OMIM:609654)
TMCO1 defect syndrome (Orphanet:228407)
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME (OMIM:601321)