Brain calcification, Rajab type

Orpha code: 178506OMIM code: 613658

Definicja

A rare, inherited disorder characterized by widespread calcifications of basal ganglia and cortex, developmental delay, small stature, retinopathy and microcephaly. The absence of progressive deterioration of the neurological functions is characteristic of the disease.

Disease data
Klasyfikacja

Disease

Kod ORPHA
178506
Kod OMIM
613658
Kod ICD10
G93.8
Kod ICD11
LD20.4

No additional description.

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