Laurence-Moon syndrome
(Q3961678)
rare autosomal recessive genetic disorder associated with retinitis pigmentosa, spastic paraplegia, and mental disabilities
rare autosomal recessive genetic disorder associated with retinitis pigmentosa, spastic paraplegia, and mental disabilities
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Current Data About
Laurence-Moon syndrome
other details
aliases |
Laurence-Moon-Biedl syndrome LAURENCE-MOON SYNDROME LNMS LAURENCE-MOON SYNDROME; LNMS |
description | rare autosomal recessive genetic disorder associated with retinitis pigmentosa, spastic paraplegia, and mental disabilities |
External Links
(P486) |
D007849
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(P492) |
245800
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(P493) |
759.89
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(P494) |
Q87.8
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(P557) |
30072
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(P646) |
/m/0d71d4
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(P665) |
H02137
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(P672) |
C10.228.140.617.500
C16.131.077.509 |
(P699) |
DOID:1930
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(P1550) |
2377
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(P2892) |
C0023138
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(P4229) |
Q87.8
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(P4317) |
12635
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(P5270) |
MONDO_0009514
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(P6366) |
2780077619
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(P11143) |
Laurence–Moon syndrome
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(P11430) |
DI-04372
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