Disease #03243 (MPMCD (myopathy, mitochondrial progressive, with congenital cataract and developmental delay), OMIM:613076)

Official abbreviation MPMCD
Name myopathy, mitochondrial progressive, with congenital cataract and developmental delay
OMIM ID 613076
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene GFER
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-01-14 16:06:18 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00074417 - PubMed: Di Fonzo 2009, Journal: Di Fonzo 2009 patient II2 M yes - Moroccan >17y - - - MPMCD psychomotor delay (HP:0001263), progressive visual deficit (HP:0000529), retinal detachment (HP:0000541), severe visual impairment (HP:0001141), severe progressive hearing loss (HP:0001730), bilateral ptosis (HP:0001488), generalized muscular hypotonia (HP:0001290), lower limb hypotrophy (HP:0008944), rotatory nystagmus (HP:0001583), no proximal (-HP:0003701) and distal muscle weakness (-HP:0002460), reduced tendon reflexes (HP:0001315), hypoferritinemia (HP:?), hyperamylasemia (HP:?), hyperCKemia (HP:?), thin corpus callosum (HP:0002079) GFER GFER 1 1 Jamie Zeegers
00074418 - PubMed: Di Fonzo 2009, Journal: Di Fonzo 2009 patient II4 M yes Morocco Moroccan >07y - - - MPMCD congenital cataract (HP:0000519), progressive axial hypotonia (HP:0008936), unilateral ptosis (HP:0007687), slight sensorineural hearing loss (HP:0000407), diffuse muscle hypotrophy (HP:0003202), hypotonia (HP:0001252), low serum ferritin (HP:?) GFER GFER 1 1 Jamie Zeegers
00074419 - PubMed: Di Fonzo 2009, Journal: Di Fonzo 2009 2-generation family, 3 affecteds (3M), unaffected heterozygous carrier parents, patient II5 M yes Morocco Moroccan >03y - - - MPMCD congenital cataract (HP:0000519), slight axial hypotonia (HP:0000519) GFER GFER 1 3 Jamie Zeegers
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