Pectus excavatum of inferior sternum
Symptom Information:
Symptom ID: | HPO:0000915 | ||||||||||||||||||||||
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 excavatum(HPO:0000767) Pectus excavatum of inferior sternum(HPO:0000915) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Thoracic disorders (excl lung and pleura)(MedDRA:10013369) Thoracic musculoskeletal disorders(MedDRA:10043475) Pectus excavatum of inferior sternum(HPO:0000915) |
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Database Frequency: | 21 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
16p13.3 microduplication syndrome | (Orphanet:96078) |
17q11 microdeletion syndrome | (Orphanet:97685) |
17q11.2 microduplication syndrome | (Orphanet:139474) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2 | (OMIM:615349) |
Fine-Lubinsky syndrome | (Orphanet:1272) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
Menkes disease | (Orphanet:565) |
Mowat-Wilson syndrome | (Orphanet:2152) |
NOONAN SYNDROME 1 | (OMIM:163950) |
NOONAN SYNDROME 4 | (OMIM:610733) |
Noonan syndrome | (Orphanet:648) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
Renpenning syndrome | (Orphanet:3242) |
SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS | (OMIM:609654) |
TMCO1 defect syndrome | (Orphanet:228407) |
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME | (OMIM:601321) |