Talipes
Symptom Information:
Symptom ID: | HPO:0001883 | |||
Synonyms: |
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Quality: | ||||
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 appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Positional foot deformity(HPO:0005656) Talipes(HPO:0001883) MedDRA: |
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Database Frequency: | 12 / 7739 | |||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
Congenital muscular dystrophy due to LMNA mutation | (Orphanet:157973) |
Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Native American myopathy | (Orphanet:168572) |
SECKEL SYNDROME 1 | (OMIM:210600) |
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES | (OMIM:615789) |
Seckel syndrome | (Orphanet:808) |
Steinert myotonic dystrophy | (Orphanet:273) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |