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Congenital diseaseGenetic abnormalityGenetic diseaseInherited diseaseInherited disorderGenopathyCongenital disorderMorphopathyFamily historyGenodermatosisBirth defectDigeorge syndromePathogeneticsDiathesisEdwards syndromeEnzymopathyPrimary immunodeficiencyChondrodystrophyDiseaseAetiopathogenesisFaciodigitogenital dysplasiaSyndromeLaminopathyNephronophthisisCiliopathyMalformationDown syndromeDysgenesisGalactosemiaStickler syndromeDysmorphologyTurner syndromePathogenesisMucopolysaccharidosisAlagille syndromeBloom's syndromeXanthinuriaOrganic defectMuscular dystrophyDown's syndromeDystrophySaccharidosisLesch-nyhan syndromeFg syndromeGangliosidosisNeurodisorderFunctional disorderStructural disorderGaucher's diseaseCharcot-marie-toothAgenesisDyspraxiaAdermatoglyphiaDysfibrinogenemiaComplaintDysseaseCri du chat syndromeAvitaminosisMorbusInfectionProgeriaPycnodysostosisRasopathyMarshall syndromeChondrodysplasiaNosogenesisBrugada syndromeCystinosisAgnogenesisTay-sachs diseaseTownes-brocks syndromeAbiotrophyEmbryofetopathyAicardi-goutières syndromePsychogenesisNeurofibromatosisNorrie diseaseLanger-giedion syndromePolychromiaGlycogenosisCardiopathyPallister-hall syndromeMarfan syndromeTrichosisOsteochondrodysplasiaCornelia de lange syndromeSpectrum disorderPathologyDown'sDravet syndromeDonohue syndromeBubble boy diseaseSotos syndromeThyroidopathyPathophenotypeHistidinemiaEmbryopathyAlymphocytosisIdiopathyAcquired disorder