Disorders: I

Disorders Alternate Names Genes Inheritance Pattern
IFAP (BRESHECK) Syndrome atrichia, BRESHECK syndrome, ichthyosis follicularis MBTPS2 X-linked recessive
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 3 ICF3 CDCA7 autosomal recessive
Incontinentia Pigmenti Bloch-Sulzberger syndrome, IP NEMO X-linked dominant
Infantile Cerebellar-Retinal Degeneration IRCD ACO2 autosomal recessive
Intellectual Disability with Dysmorphic Facies and Ptosis IDDDFP BRPF1 autosomal dominant
Iridogoniodysgenesis and Skeletal Anomalies ? autosomal recessive
Iridogoniodysgenesis, Type 1 autosomal dominant iridogoniodysgenesis anomaly, IGDA, IRID1, iris hypoplasia with glaucoma FOXC1 autosomal dominant
Iridogoniodysgenesis, Type 2 IGDS, IHGA, IRID2, iridogoniodysgenesis syndrome, iris hypoplasia with early-onset glaucoma PITX2 autosomal dominant