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Total number of diseases with letter "I" in database: 100

A -B -C -D -E -F -G -H -I -J -K -L -M -N -O -P -Q -R -S -T -U -V -W -X -Y - Z

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Immunodeficiency, microcephaly, and chromosomal instability
Immunodeficiency, polyendocrinopathy, and enteropathy, X-linked
Immunodeficiency, X-linked progressive combined variable
Immunodysregulation polyendocrinopathy and enteropathy X-linked/IPEX
Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked (IPEX)
Immunoglobulin Gm1
IMPDH1-Related Retinitis Pigmentosa
Inclusion body myopathy 2, autosomal recessive (IBM2)
Inclusion body myopathy, autosomal recessive
Inclusion body myopathy, quadriceps-sparing (QSM)
Incontinentia pigmenti
Incontinentia pigmenti (IP)
Incontinentia pigmenti, familial male-lethal type
Incontinentia pigmenti, type II (IP2)
Infantile neuronal ceroid lipofuscinosis (INCL)

Should you not find the disease for which you are searching, please send an email to EDDNAL: eddnal@skypro.be

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