H00039  Basal cell carcinoma
     H00267  Holoprosencephaly
     H00263  Acrocallosal syndrome
     H01835  Neuronal migration disorder
     H01027  Microphthalmia
     H00482  Brachydactyly
     H01852  Postaxial polydactyly
     H02332  Preaxial polydactyly
     H00530  Joubert syndrome and related disorders
     H00675  Acrocapitofemoral dysplasia
     H02158  Weyers acrofacial dysostosis
     H02161  Greig cephalopolysyndactyly syndrome
     H00503  Ellis-van Creveld syndrome
     H00895  Basal cell nevus syndrome
     H00502  Pallister-Hall syndrome
     H00886  Donnai-Barrow syndrome
     H01265  Hydrolethalus syndrome
     H02479  Nivelon-Nivelon-Mabille syndrome

     H00014  Non-small cell lung cancer
     H00013  Small cell lung cancer
     H02308  Immunodeficiency-centromeric instability-facial anomalies syndrome
     H00480  X-linked intellectual developmental disorder
     H00773  Autosomal dominant intellectual developmental disorder
     H00606  Early infantile epileptic encephalopathy
     H00591  Facioscapulohumeral muscular dystrophy
     H02122  Chronic atrial and intestinal dysrhythmia
     H00269  Primary microcephaly
     H00267  Holoprosencephaly
     H02707  Khan-Khan-Katsanis syndrome
     H01734  Rothmund-Thomson syndrome
     H00572  Roberts-SC phocomelia syndrome
     H00631  Cornelia de Lange syndrome
     H00914  Warsaw breakage syndrome
     H02581  Juberg-Hayward syndrome
     H01752  ATR-X syndrome
     H02460  Neurodevelopmental disorder with dysmorphic facies and skeletal anomalies
     H02582  Mullegama-Klein-Martinez syndrome
     H02583  X-linked intellectual disability-hypotonic facies syndrome
     H02584  Ferguson-Bonni neurodevelopmental syndrome
     H02632  PP2A-related neurodevelopmental disorder