Disease Index

(9q34.3).

human disease

medical condition

syndrome characterized by malar and mandibular hypoplasia, typically associated with abnormalities of the ears and eyelids, and with alopecia

human disease

autosomal dominant disease characterized by progressive microcephaly, micrognathia, microtia, dysplastic ears, preauricular skin tags, speech delay, significant developmental delay, midface and malar hypoplasia,

human disease

manganese poisoning

Lysosomal storage disease

parasitic infection by nematodes transmitted by insects

B-cell lymphocytic neoplasm due to CD5 positive antigen-naive pregerminal center B-cell within the mantle zone that surrounds normal germinal center follicles

human disease

human disease

human disease

medical condition

medical condition

genetic disorder of the connective tissue

hypothesized form of Marfan; dubious

human disease

human disease

human disease

human disease

group of lymphomas

disease

human disease

Marinesco-Sjogren syndrome (MSS) belongs to the group of autosomal recessive cerebellar ataxias. Cardinal features of MSS are cerebellar ataxia, congenital cataract, and delayed psychomotor development.