Disease Browser
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Parent Node: Chromosome Deletion (D002872) | ..Starting node ..Chromosome 9p Deletion Syndrome (C538024)
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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)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 2355 |
Name: | Chromosome 9p Deletion Syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D002872 |
TreeNumbers: | C23.550.210.050.500.500/C538024 |
Synonyms: | Chromosome 9, monosomy 9p |Monosomy 9p |Monosomy 9p Syndrome |
Slim Mappings: | Pathology (process) |
Reference: |
MedGen: C538024
MeSH: C538024
OMIM: 158170;
Genes: AF8T; | Phenotypes | | Disease Causing ClinVar Variants | |
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