NDUFB11-related disorders

MONDO:1040023

A group of rare genetic conditions caused by variants in the NDUFB11 gene. Presentation is heterogenous including neurologic, cardiac, ocular, and dermatological abnormalities.

0 clinical trials for this condition and its sub-types, 0 tagged with NDUFB11-related disorders itself.

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Part of

↑ Hereditary disease (18187) ↑ Syndromic disease (7133)

Sub-types of NDUFB11-related disorders

Linear skin defects with multiple congenital anomalies 3 0 trials
Mitochondrial complex I deficiency, nuclear type 30 0 trials

Including sub-types (0) Tagged with NDUFB11-related disorders (0)

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