Disease Index
9,486 diseaseschromosome 19p13.13 deletion syndrome
Human disease
chromosome 19q13.11 deletion syndrome
Human disease
MeSH: C567810
chromosome 1p32-p31 deletion syndrome
Human disease
chromosome 1p36 deletion syndrome
Human disease
MeSH: C535362
chromosome 1q21.1 deletion syndrome
Human disease
chromosome 1q21.1 duplication syndrome
Human disease
MeSH: C567290
chromosome 1q41-q42 deletion syndrome
Human disease
chromosome 22q11.2 microduplication syndrome
Human disease
MeSH: C567224
chromosome 2q deletion
human disease
chromosome 2q32-q33 deletion syndrome
Human disease
MeSH: C567350
chromosome 3q13.31 deletion syndrome
Human disease
MeSH: C536808
chromosome 3q29 microdeletion syndrome
Human disease
MeSH: C567184
chromosome 3q29 microduplication syndrome
Human disease
MeSH: C567626
chromosome 4q21 deletion syndrome
Human disease
chromosome 5p13 duplication syndrome
Human disease
MeSH: C567717
chromosome 5q deletion syndrome
human disease
MeSH: C535323
chromosome 5q12 deletion syndrome
Human disease
chromosome 6pter-p24 deletion syndrome
Human disease
MeSH: C567239
chromosome 6q24-q25 deletion syndrome
Human disease
chromosome 8-derived supernumerary ring/marker
MeSH: C537824
chromosome 8q21.11 deletion syndrome
Human disease
chromosome 9p deletion syndrome
Human disease
MeSH: C538024
chromosome abnormality
abnormal number or structure of chromosomes
MeSH: D002869
chromosome X structural anomaly
human disease
chromosome Xp11.23-p11.22 duplication syndrome
Human disease
MeSH: C567585
chromosome Xp21 deletion syndrome
Human disease
chromosome Y structural anomaly
human disease
chronic acquired demyelinating polyneuropathy
human disease
chronic actinic dermatitis
. Resolution of photosensitivity is reported in up to 50% of individuals after 15 years or more, with contact allergies persisting.
ICD: L57.1
chronic atrial and intestinal dysrhythmia
Human disease