Saethre-Chotzen syndrome
(Q3508686)
acrocephalosyndactylia that has material basis in a genetic mutation in the TWIST1 gene which results in premature fusion located in skull
acrocephalosyndactylia that has material basis in a genetic mutation in the TWIST1 gene which results in premature fusion located in skull
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Current Data About
Saethre-Chotzen syndrome
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q1786496)
(Q200779)
(Q18553439)
(Q12136) |
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| (P373) |
Saethre-Chotzen syndrome
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| (P460) |
(Q55950182)
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| (P667) |
A90
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| (P780) |
(Q378183)
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| (P1748) |
C75034
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| (P1995) |
(Q327657)
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| (P2293) |
(Q14906427)
(Q14911644)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_14768
http://identifiers.org/doid/DOID:14768
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| (P5008) |
(Q4099686)
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other details
| aliases |
acrocephalosyndactyly type III Saethre–Chotzen syndrome SCS |
| description | acrocephalosyndactylia that has material basis in a genetic mutation in the TWIST1 gene which results in premature fusion located in skull |
External Links