Disease #00042 (DS (Down Syndrome), OMIM:190685)

Official abbreviation DS
Name Down Syndrome
OMIM ID 190685
Human Phenotype Ontology Project (HPO) HPO
Inheritance Isolated Cases (Sporadic)
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GATA1
Associated tissues -
Disease features -
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00000247 Su Han Lum et al. (2016) - Malaysia - - - - DS Associated with transient abnormal myelopoiesis (TAM) GATA1 GATA1 6 1 Nuur Athirah Binti Mohd Daud
00000248 Su Han Lum et al. (2016) - Malaysia - - - - DS Associated with myeloid leukemia of DS (ML-DS) GATA1 GATA1 7 1 Nuur Athirah Binti Mohd Daud
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