(Q1457267)

Malformations of Cortical Development, Group III

28 July 2018

0 references

0 references

0 references

Encephaloclastic disorder

1 reference

cerebral malformation with epilepsy

28 July 2018

Mondo ID

MONDO_0010011

1 reference

Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly

28 July 2018

0 references

0 references

2 references

13 August 2019

2 references

13 August 2019

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

1 reference

13 August 2019

1 reference

Maternally inherited heterozygous sequence change in the sonic hedgehog gene in a male patient with bilateral closed-lip schizencephaly and partial absence of the corpus callosum.

ICD-9-CM

742.4

1 reference

28 July 2018

C99056

exact match

1 reference

http://purl.obolibrary.org/obo/HP_0010636

28 July 2018

1 reference

8 October 2018

http://www.orpha.net/ORDO/Orphanet_799

0 references

Commons category

Schizencephaly

0 references

Identifiers

MeSH descriptor ID

D065707

subject named as

Schizencephaly

1 reference

8 October 2018

PatientsLikeMe condition ID

MeSH tree code

C10.500.507.500.750

0 references

C16.131.666.507.500.750

0 references

0 references

0 references

0 references

1 reference

eMedicine ID

413051

1 reference

Encyclopædia Britannica Online ID

science/schizencephaly

subject named as

schizencephaly

0 references

1 reference

28 October 2013

0 references

1 reference

8 October 2018

ICD-10

Q04.6

1 reference

1 reference

28 July 2018

0 references

LA05.61

Schizencephaly

0 references

ICD-9 ID

742.4

1 reference

Microsoft Academic ID

0 references

0 references

exact match

2 references

https://docs.openalex.org/download-snapshot/snapshot-data-format

28 July 2018

1 reference

26 January 2022

Orphanet ID

799

exact match

1 reference

28 July 2018

1 reference

close match

1 reference

28 July 2018

1 reference

8 October 2018