Coxa magna
Symptom Information:
Symptom ID: | HPO:0003279 | ||
Synonyms: |
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Cross references: |
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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 joint morphology(HPO:0001367) Abnormality of lower limb joint(HPO:0100491) Abnormality of the hip bone(HPO:0003272) Coxa magna(HPO:0003279) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of pelvic girdle bone morphology(HPO:0002644) Abnormality of the hip bone(HPO:0003272) Coxa magna(HPO:0003279) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the lower limb(HPO:0002814) Abnormality of lower limb joint(HPO:0100491) Abnormality of the hip bone(HPO:0003272) Coxa magna(HPO:0003279) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE III | (OMIM:190351) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |