Wolf-Hirschhorn syndrome
(Q610075)
chromosome abnormality with a distinct craniofacial phenotype and intellectual disability
chromosome abnormality with a distinct craniofacial phenotype and intellectual disability
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Current Data About
Wolf-Hirschhorn syndrome
| (P18) |
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| (P31) |
(Q112193867)
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| (P138) |
(Q280337)
(Q2476950) |
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| (P279) |
(Q16918398)
(Q55786590) (Q12136) |
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| (P373) |
Wolf–Hirschhorn syndrome
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| (P1748) |
C35528
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| (P1995) |
(Q1071953)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0050460
http://identifiers.org/doid/DOID:0050460
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| (P5008) |
(Q4099686)
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other details
| aliases |
4p deletion syndrome chromosome deletion Dillan 4p syndrome Pitt syndrome Pitt–Rogers–Danks syndrome WHS PRDS Pitt-Rogers-Danks Syndrome chromosome 4p16.3 deletion syndrome Wolf–Hirschhorn syndrome Dillan 4p syndrome 4p-syndrome |
| description | chromosome abnormality with a distinct craniofacial phenotype and intellectual disability |
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