Skip to main content

Clinical Disorder Search

Terms: night blindness, jaundice, cataracts, etc.
3 | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | R | S | T | U | V | W | Z

Reset

I
Disorder Name Genes Alternate Names OMIM Inheritance
IFAP (BRESHECK) Syndrome MBTPS2 atrichia, ichthyosis follicularis, BRESHECK syndrome 308205 X-linked recessive
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 3 CDCA7 ICF3 616910 autosomal recessive
Incontinentia Pigmenti NEMO Bloch-Sulzberger syndrome, IP 308300 X-linked dominant
Infantile Cerebellar-Retinal Degeneration ACO2 IRCD 614559 autosomal recessive
Intellectual Disability with Dysmorphic Facies and Ptosis BRPF1 IDDDFP 617333 autosomal dominant
Iridogoniodysgenesis and Skeletal Anomalies ? 609515 autosomal recessive
Iridogoniodysgenesis, Type 1 FOXC1 IRID1, IGDA, anterior segment dysgenesis 3, autosomal dominant iridogoniodysgenesis anomaly, iris hypoplasia with glaucoma 601631 autosomal dominant
Iridogoniodysgenesis, Type 2 PITX2 IRID2, IGDS, iridogoniodysgenesis syndrome, anterior segment dysgenesis 4, iris hypoplasia with early-onset glaucoma, IHGA 137600 autosomal dominant