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Achromatopsia
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Alagille syndrome
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Deafness_IsolatedAndComplex
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IBMDx study
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Incidentalome_PREGEN_DRAFT
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Kabuki syndrome
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Kidneyome_SuperPanel
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Liverome Superpanel
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Mackenzie's Mission_Reproductive Carrier Screening
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Myopathy Superpanel
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Photosensitivity Syndromes
Pierre Robin Sequence
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Prepair 1000+
Prepair 500+
Primary nodular adrenocortical disease
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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
Retinitis pigmentosa
Rhabdomyolysis and Metabolic Myopathy
Sarcoma non-soft tissue
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Schwannoma
Severe Combined Immunodeficiency
Severe early-onset obesity
Short QT syndrome
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Skeletal Dysplasia_Fetal
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Speech apraxia
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Stickler Syndrome
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Susceptibility to Viral Infections
Syndromic Retinopathy
Thyroid Cancer
Transplant Co-Morbidity
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
Tubulinopathies
Usher Syndrome
Vascular Malformations_Germline
Vascular Malformations_Somatic
Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
Panel Version
2.10
1.5025
Gene or Genomic Entity Name
CFAP251
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07 Jun 2026
Mendeliome v2.0
CFAP251
Gene symbol changed from WDR66 to CFAP251 during gene set migration (ENSG00000158023 -> ENSG00000158023)