All individuals with variants in gene CPZ

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00213475 30609410-FamDM516Pat PubMed: Khan 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F - Mexico Mexican 00y04m - - - ? microcephaly (HP:0000252), micrognathia (HP:0000347), arched eyebrows (HP:0002553); hypertonia (HP:0001276), low-lying conus medullaris (HP:0002143); hydronephrosis (HP:0000126), small kidneys (HP:0000089); vision loss (HP:0000572), Peters anomaly (HP:0000659), glaucoma (HP:0000501), buphthalmos (HP:0000557); clinodactyly, fifth finger, right hand (HP:0030084), absent fourth and fifth digits, left foot; absent fifth digit, right foot (HP:0006209), contractures of left arm and leg (HP:0001371), Intrauterine growth restriction (HP:0001511), small for gestational age (HP:0001518), failure to thrive (HP:0001508), sacral dimple (HP:0000960), patent ductus arteriosus after premature birth (HP:0011649), patent foramen ovale (HP:0001655), tricuspid regurgitation (HP:0005180), heart murmur (HP:0030148), bilateral superior vena cava with no bridging vein (HP:0011668), anemia (HP:0001903), lymphopenia (HP:0001888), neutropenia (HP:0001875), oral-pharyngeal dysphagia (HP:0200136); 4m-deceased 2 1 Johan den Dunnen
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