Disease #05347 (MISSLA (microcephaly, short stature, limb abnormalities (MISSLA)), OMIM:617604)

Official abbreviation MISSLA
Name microcephaly, short stature, limb abnormalities (MISSLA)
OMIM ID 617604
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene DONSON
Associated tissues -
Disease features -
Remarks autosomal recessive
Date created 2017-11-17 14:46:08 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00134048 - - 2 generation family, 2 affecteds (2F), 4 unaffecteds (3M, 1F) F no Germany European - - - - MISSLA - DONSON DONSON 2 1 Martin Atta Mensah
00207473 - - - F no Germany - - - - - MISSLA - DONSON DONSON 2 2 Martin Atta Mensah
00433154 199808 - - F ? Syria - - - - - MISSLA Microcephaly, Neurodevelopmental abnormality, Migraine without aura, Abnormal cortical gyration, Hypotonia, Decreased body mass index, Subcortical heterotopia, Intellectual disability, Delayed speech and language development DONSON DONSON 2 1 Andreas Laner
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