All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04549 KMT2A leukemia, myeloid/lymphoid or mixed-lineage (KMT-2A) 159555 - - - KMT2A - -
02534 WDSTS Wiedemann-Steiner syndrome 605130 PG 49 48 KMT2A - thick eyebrows, synophrys and thick eyelashes with vertically narrow and down-slanting palpebral fissures.   global developmental delay (HP:0001263); intellectual disability (HP:0001249); seizure (HP:0001250); hypotonia (HP:0001252); short stature (HP:0004322); no obesity (-HP:0001513); digital abnormalities (HP_0011297); hypertrichosis over their forearms, legs and back
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