Disease #05535 (macrocephaly (macrocephaly))

Official abbreviation macrocephaly
Name macrocephaly
OMIM ID -
Inheritance Isolated Cases (Sporadic)
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2018-12-22 14:33:20 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00209038 28771251-Pat84 PubMed: Lionel 2018 - M - Canada - - - - - macrocephaly Macrocephaly, developmental delay, and ketotic hypoglycemiaa PTEN PTEN 1 1 Johan den Dunnen
00210372 139648 - - M ? Finland - - - - - macrocephaly macrocephaly + 3.7 SD at age 1,5y, developmental delay PTEN PTEN 1 1 Andreas Laner
00373335 Proband1 Singh R and Cohen ASA, et al. Cold Spring Harb Mol Case Stud, 2021. - M - United States - - - - - CRS, DD, macrocephaly - - - 1 1 Stuart Scott
00452066 - - - F - - (not applicable) white - - - - macrocephaly HP:0000256, HP:0005490, HP:0001520 - CHD8 1 1 Marketa Wayhelova
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