du Pan syndrome
bone malformation affecting arms and legs
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du Pan syndrome
Summary
du Pan syndrome is a genetic disease[1].
Key Facts
- du Pan syndrome's instance of is recorded as genetic disease[2].
- du Pan syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- du Pan syndrome's instance of is recorded as rare disease[4].
- du Pan syndrome's instance of is recorded as class of disease[5].
- du Pan syndrome is a type of acromesomelic dysplasia[6].
- du Pan syndrome is a type of autosomal recessive disease[7].
- du Pan syndrome is a type of syndrome with limb reduction defects[8].
- du Pan syndrome is a type of dysostosis of genetic origin with limb anomaly as a major feature[9].
- du Pan syndrome is a type of bone disease[10].
- du Pan syndrome is a type of bone development disease[11].
- du Pan syndrome's Commons category is recorded as Du Pan syndrome[12].
- du Pan syndrome's anatomical location is recorded as bone[13].
- du Pan syndrome's genetic association is recorded as GDF5[14].
- du Pan syndrome's genetic association is recorded as BMPR1B[15].
- du Pan syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050790[16].
- du Pan syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050790[17].
- du Pan syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].