Seckel syndrome
(Q572169)
autosomal recessive disease characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability
autosomal recessive disease characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability
Language:
Current Data About
Seckel syndrome
(P31) |
(Q929833)
(Q112193867) |
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(P279) |
(Q10267817)
(Q2289761) (Q179630)
(Q12136) |
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(P1748) |
C125488
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(P1995) |
(Q1071953)
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(P2293) |
(Q14908120)
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(P2888) |
http://purl.obolibrary.org/obo/DOID_0050569
http://identifiers.org/doid/DOID:0050569
http://www.orpha.net/ORDO/Orphanet_808 |
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(P5008) |
(Q4099686)
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other details
aliases |
Virchow-Seckel syndrome Harper's syndrome Virchow-Seckel dwarfism bird-headed dwarfism microcephalic primordial dwarfism Virchow–Seckel dwarfism bird-headed dwarf of Seckel |
description | autosomal recessive disease characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability |
External Links
(P492) |
210600
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(P493) |
759.89
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(P557) |
31625
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(P646) |
/m/0cd6h_
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(P665) |
H00992
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(P699) |
DOID:0050569
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(P1550) |
808
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(P4229) |
Q87.1
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(P4317) |
8562
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(P6366) |
2778565148
|
(P11143) |
Seckel syndrome
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