Disease Browser
Parent Node: Anemia, Macrocytic (D000748) Parent Node: Chromosome Deletion (D002872) ..Starting node .. 5q- syndrome (C535323) Child Nodes:
Sister Nodes: ..10p Deletion Syndrome (Partial) (C538288) ..13q deletion syndrome (C535484) 1 ..15q24 Microdeletion (C579849) ..16p11.2 Deletion Syndrome (C579850) ..5q- syndrome (C535323) ..7p2 monosomy syndrome (C537818) ..Chromosome 1, deletion q21 q25 (C535363) ..Chromosome 1, monosomy 1p (C535591) ..Chromosome 1, monosomy 1p22 p13 (C535592) ..Chromosome 1, monosomy 1p31 p22 (C535593) ..Chromosome 1, monosomy 1p32 (C535594) ..Chromosome 1, monosomy 1p34 p32 (C535595) ..Chromosome 1, monosomy 1q25 q32 (C535596) ..Chromosome 1, monosomy 1q32 q42 (C537671) ..Chromosome 1, monosomy 1q4 (C537672) ..Chromosome 10, monosomy 10q (C538289) ..Chromosome 10q23 Deletion Syndrome (C567385) ..Chromosome 10q26 Deletion Syndrome (C567182) ..Chromosome 11, deletion 11p (C538293) ..Chromosome 11p Deletion Syndrome (C541598) ..Chromosome 11p, partial deletion (C538295) ..Chromosome 11q partial deletion (C538296) ..Chromosome 12p deletion (C538301) ..Chromosome 12p partial deletion (C538302) ..Chromosome 14q, partial deletions (C538031) ..Chromosome 14q, terminal deletion (C538033) ..Chromosome 15q, partial deletion (C538038) ..Chromosome 15q13.3 Microdeletion Syndrome (C567439) ..Chromosome 17 deletion (C538045) 1 ..Chromosome 17, deletion 17q23 q24 (C538047) ..Chromosome 17q21.31 Deletion Syndrome (C566476) ..Chromosome 18 deletion syndrome (C536580) ..Chromosome 18, deletion 18q23 (C538305) ..Chromosome 18p deletion syndrome (C538309) ..Chromosome 19q13.11 Deletion Syndrome (C567810) ..Chromosome 1p36 Deletion Syndrome (C535362) ..Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb (C567291) ..Chromosome 1q21.1 Duplication Syndrome (C567290) ..Chromosome 1q43-Q44 Deletion Syndrome (C567346) ..Chromosome 2, monosomy 2p22 (C538313) ..Chromosome 2, monosomy 2pter p24 (C538314) ..Chromosome 2, monosomy 2q (C538315) ..Chromosome 2, monosomy 2q24 (C538316) ..Chromosome 20, deletion 20p (C535370) ..Chromosome 21, monosomy 21q22 (C537110) ..Chromosome 22, microdeletion 22 q11 (C536797) ..Chromosome 22q11.2 Deletion Syndrome, Distal (C567511) ..Chromosome 2p16.1-P15 Deletion Syndrome (C567289) ..Chromosome 2q31.2 Deletion Syndrome (C567344) ..Chromosome 2q32-Q33 Deletion Syndrome (C567350) ..Chromosome 2q37 deletion syndrome (C538317) 1 ..Chromosome 3, monosomy 3p (C536804) ..Chromosome 3, monosomy 3p14 p11 (C536805) ..Chromosome 3, monosomy 3p2 (C536806) ..Chromosome 3, monosomy 3p25 (C536807) ..Chromosome 3, monosomy 3q13 (C536808) ..Chromosome 3, monosomy 3q21 23 (C536809) ..Chromosome 3, monosomy 3q27 (C536810) ..CHROMOSOME 3pter-p25 DELETION SYNDROME (OMIM:613792) ..Chromosome 3q29 Deletion Syndrome (C567184) ..Chromosome 4 short arm deletion (C537637) ..Chromosome 4, 4q Terminal Deletion Syndrome (C537641) ..Chromosome 4, monosomy 4p14 p16 (C537638) ..Chromosome 4, monosomy 4q32 (C537640) ..Chromosome 4q- Syndrome (C537639) ..Chromosome 6, deletion 6q13 q15 (C537764) ..Chromosome 6, monosomy 6p23 (C537765) ..Chromosome 6, monosomy 6q (C537807) ..Chromosome 6, monosomy 6q1 (C537808) ..Chromosome 6, monosomy 6q2 (C537809) ..Chromosome 6pter-P24 Deletion Syndrome (C567239) ..Chromosome 7, monosomy (C537814) ..Chromosome 7, monosomy 7q2 (C537815) ..Chromosome 7, monosomy 7q21 (C537816) ..Chromosome 7, monosomy 7q3 (C537817) ..CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB (OMIM:613729) ..Chromosome 8, monosomy 8p (C537825) ..Chromosome 8, monosomy 8p23 1 (C537827) ..Chromosome 8, monosomy 8q (C537828) ..Chromosome 8p deletion syndrome (partial) (C537826) ..CHROMOSOME 8q21.11 DELETION SYNDROME (OMIM:614230) ..Chromosome 9, partial monosomy 9p (C538025) ..Chromosome 9p Deletion Syndrome (C538024) ..Deafness, Sensorineural, And Male Infertility (C567010) ..Deletion 13q syndrome, partial (C535449) ..Deletion 6q16 q21 (C538207) ..Fragile Site 16p12 (C565001) ..Holoprosencephaly 10 (C567278) ..Homozygous 11p15-p14 Deletion Syndrome (C564701) ..Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia (C565016) ..Hypotonia-Cystinuria Syndrome (C564710) ..Kleefstra Syndrome (C563043) ..Male sterility due to Y-chromosome deletions (C536297) ..Monosomy 7 of Bone Marrow (C565370) ..NF1 Microdeletion Syndrome (C563524) ..Otodental Dysplasia (C563482) ..Potocki-Shaffer syndrome (C538356) ..Prader-Willi-Like Syndrome Associated With Chromosome 6 (C566764) ..Telomeric 22q13 Monosomy Syndrome (C536801) ..X chromosome, monosomy Xp22 pter (C536754) ..X chromosome, monosomy Xq28 (C536755) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD