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

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000054269 congenital cataract (HP:0000519), slight axial hypotonia (HP:0000519) - - Familial, autosomal recessive 03y - - - - Jamie Zeegers 00074419
0000054270 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:?) - - Familial, autosomal recessive 07y - - - - Jamie Zeegers 00074418
0000054271 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) - - Familial, autosomal recessive 17y - 00y01m axial hypotonia (HP:0008936), congenital cataract (HP:0000519) - Jamie Zeegers 00074417
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