Disease #02650 (FCORD-2 (dysplasia, cortical, focal type II (FCORD-2)), OMIM:607341)

Official abbreviation FCORD-2
Name dysplasia, cortical, focal type II (FCORD-2)
OMIM ID 607341
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 0
Associated with 3 genes MTOR, TSC1, TSC2
Associated tissues -
Disease features -
Remarks -


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00226318 patient1 - - F ? ? (unknown) - - 0 - - FCORD-2 - DEPDC5 DEPDC5 1 1 Lisa-Marie Niestroj
00226327 patient3 - - F ? ? (unknown) - - 0 - - FCORD-2 - NPRL3 NPRL3 1 1 Lisa-Marie Niestroj
00226335 patient5 - - F - - - - 0 - - FCORD-2 - MTOR MTOR 1 1 Lisa-Marie Niestroj
00234381 - - - F - - - - 0 - - FCORD-2 - - RHEB 1 1 Lisa-Marie Niestroj
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