Superior pectus carinatum
Symptom Information:
Symptom ID: | HPO:0000917 | ||||||||||||||||
Synonyms: |
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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 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) |
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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) |