Warburg micro syndrome
(Q6839205)
autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism
autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism
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Current Data About
Warburg micro syndrome
| (P31) |
(Q929833)
(Q112193867) |
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| (P138) |
(Q19731788)
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| (P279) |
(Q10267817)
(Q179630)
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| (P2293) |
(Q18036602)
(Q18036603)
(Q18037685)
(Q18049892)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0060237
http://identifiers.org/doid/DOID:0060237
http://www.orpha.net/ORDO/Orphanet_2510 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
WARBM Warburg-Sjo-Fledelius syndrome micro syndrome Warburg micro-syndrome |
| description | autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism |
External Links
| (P486) |
C536681
|
| (P492) |
600118
|
| (P665) |
H00792
|
| (P699) |
DOID:0060237
|
| (P1550) |
2510
|
| (P2892) |
C1838625
|
| (P4317) |
5534
|
| (P6366) |
2780565095
|
| (P11143) |
Warburg Micro syndrome
|