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PAPA6
MCID: PLY101
MIFTS: 15
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Polydactyly, Postaxial, Type A6 (PAPA6)
Categories:
Bone diseases, Fetal diseases, Genetic diseases, Rare diseases, Skin diseases
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MalaCards integrated aliases for Polydactyly, Postaxial, Type A6:
Characteristics:OMIM:56
Inheritance:
autosomal recessive
Miscellaneous:
reported in 1 family (last curated may 2013) variable degree of severity of widening and deviation of fifth fingers, both within and between affected individuals HPO:31Classifications:
MalaCards categories:
Global: Genetic diseases Fetal diseases Rare diseases Anatomical: Bone diseases Skin diseases |
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UniProtKB/Swiss-Prot :
73
Polydactyly, postaxial A6: A condition characterized by the occurrence of supernumerary digits in the upper and/or lower extremities. In postaxial polydactyly type A, the extra digit is well-formed and articulates with the fifth or a sixth metacarpal/metatarsal.
MalaCards based summary : Polydactyly, Postaxial, Type A6, is also known as papa6. An important gene associated with Polydactyly, Postaxial, Type A6 is ZNF141 (Zinc Finger Protein 141). Related phenotypes are postaxial hand polydactyly and broad phalanges of the 5th finger |
Human phenotypes related to Polydactyly, Postaxial, Type A6:31 (showing 2, show less)
Symptoms via clinical synopsis from OMIM:56Clinical features from OMIM:615226 |
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Articles related to Polydactyly, Postaxial, Type A6:(showing 1, show less)
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Genes related to Polydactyly, Postaxial, Type A6 (1 elite genes):(showing 1, show less) - Elite gene
- Cancer Census gene in COSMIC
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ClinVar genetic disease variations for Polydactyly, Postaxial, Type A6:6 (showing 1, show less)
UniProtKB/Swiss-Prot genetic disease variations for Polydactyly, Postaxial, Type A6:73 (showing 1, show less)
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Search
GEO
for disease gene expression data for Polydactyly, Postaxial, Type A6.
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