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
07097 HDAC3-NDD HDAC3-related NDD - IC - - HDAC3 - intellectual disability (HP:0001249),neurodevelopmental delay (HP:0012758), abnormality of the musculoskele tal system (HP:0033127), seizure (HP:0001250), abnormal facial shape (HP:0001999), brain imaging abnormality (HP:0410263), abnormality of the genitourinary system (HP:0000119), microcephaly (HP:0000252), hearing impairment (HP:0000365), failure to thrive (HP:0001508), abnormal heart morphology (HP:0001627), autistic behavior (HP:0000729)
05611 NDD neurodevelopmental disorder (NDD) - - 3730 3545 ACBD6, ADARB1, AP1G1, ARFGEF1, ATP9A, CAMSAP1, CAPRIN1, CASP2, CHASERR, CPSF3L, DDB1, DENND5B, DHX30, DHX9, DOHH, DOT1L, EEFSEC, EIF2C1, EIF2C2, EIF4A2, 72 more - -
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