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Structural eye disease v1.93 NDUFB11 Ivone Leong Mode of inheritance for gene: NDUFB11 was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Structural eye disease v0.91 NDUFB11 Nicola Ragge reviewed gene: NDUFB11: Rating: RED; Mode of pathogenicity: ; Publications: 25772934; Phenotypes: ; Mode of inheritance:
Structural eye disease v0.89 NDUFB11 Ivone Leong Source NHS GMS was added to NDUFB11.
Source Expert Review Red was added to NDUFB11.
Publications for gene NDUFB11 were changed from to 25772934
Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
Structural eye disease v0.88 NDUFB11 Ivone Leong Source Expert Review Amber was added to NDUFB11.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Structural eye disease v0.60 NDUFB11 Mariya Moosajee reviewed gene: NDUFB11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Linear Skin Defects with Multiple Congenital Anomalies 3, LSDMCA3; Mode of inheritance:
Structural eye disease v0.59 NDUFB11 Ivone Leong gene: NDUFB11 was added
gene: NDUFB11 was added to Structural eye disease. Sources: London North GLH
Mode of inheritance for gene: NDUFB11 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes for gene: NDUFB11 were set to Linear Skin Defects with Multiple Congenital Anomalies 3, LSDMCA3, 300952