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Items: 2

1.

Macular dystrophy with central cone involvement

MedGen UID:
863808
Concept ID:
C4015371
Disease or Syndrome
2.

Neuronal ceroid lipofuscinosis 7

The neuronal ceroid lipofuscinoses (NCL, or CLN) are a clinically and genetically heterogeneous group of neurodegenerative disorders characterized by the intracellular accumulation of autofluorescent lipopigment storage material in different patterns ultrastructurally (summary by Mole et al., 2005). For a general phenotypic description and a discussion of genetic heterogeneity of CLN, see CLN1 (256730). [from OMIM]

MedGen UID:
325457
Concept ID:
C1838571
Disease or Syndrome

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