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Genetic Disorders and the Fetus


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Hypogonadotropic hypogonadism 1 with or without anosmia (HH1) ANOS1 XL 1 1 2 2 0 0 Hypogonadotropic hypogonadism 1 with or without anosmia (HH1) KAL1 XL 1 2 1 1 1 1 Hypoparathyroidism–retardation–dysmorphism syndrome (HRDS) TBCE 1R 1 1 1 2 0 0 Hypophosphatasia, infantile ALPL AR 6 7 6 9 4 4 Ichthyosis, congenital, autosomal recessive 1 (ARCI1) TGM1 AD 2 9 7 10 1 1 Ichthyosis, lamellar, 2 (LI2) ABCA12 AR 2 2 1 2 0 0 Ichthyosis, spastic quadriplegia, and mental retardation (ISQMR) ELOVL4 AR 1 1 1 1 0 0 Ichthyosis, X‐linked (XLI) STS XL 2 3 3 4 1 1 Ifap syndrome with or without Bresheck syndrome MBTPS2 XL 2 3 2 5 2 1 Immunodeficiency with hyper‐IgM, type 1 (HIGM1) CD40LG XL 4 14 14 22 6 6 Immunodysregulation, polyendocrinopathy, and enteropathy, X‐linked (IPEX) FOXP3 XL 2 3 3 3 1 1 Incontinentia pigmenti (IP) IKBKG XL 15 35 28 43 11 11 Infantile cerebellar‐retinal degeneration (ICRD) ACO2 AR 1 1 1 2 2 2 Infantile liver failure syndrome 1 (ILFS1) LARS AR 1 1 2 2 1 1 Isovaleric acidemia (IVA) IVD AR 1 1 1 2 0 0 Joubert syndrome 1 (JBTS1) INPP5E AR 1 1 2 2 1 1 Joubert syndrome 17 (JBTS17) CPLANE1 AD 1 1 1 2 1 1 Joubert syndrome 2 (JBTS2) TMEM216 AR 1 1 2 2 1 1 Joubert syndrome 21 (JBTS21) CSPP1 AR 2 5 4 7 1 1 Joubert syndrome 23 (JBTS23) KIAA0586