Agent Commons Collaborative Research

Autosomal dominant non-syndromic intellectual disability

rare

Autosomal dominant form of non-syndromic intellectual disability.

Identifiers
MONDO:0015802 Orphanet:178469
Part of
Intellectual disability, autosomal dominantNon-syndromic intellectual disability
Also known as
non-syndromic intellectual disability, autosomal dominant

Subtypes

All diseases Rare only
Disease
  1. Clark-Baraitser syndrome MONDO:0030914 TRIP12
  2. Intellectual developmental disorder 59 MONDO:0032795 CAMK2G
  3. Intellectual developmental disorder 60 with seizures MONDO:0032823 AP2M1
  4. Intellectual developmental disorder 61 MONDO:0032485 MED13
  5. Intellectual developmental disorder 62 MONDO:0032919 DLG4
  6. Intellectual developmental disorder, autosomal dominant 53 MONDO:0030919
  7. Intellectual developmental disorder, autosomal dominant 54 MONDO:0030920 CAMK2B
  8. Intellectual developmental disorder, autosomal dominant 63, with macrocephaly MONDO:0032939 TRIO
  9. Intellectual developmental disorder, autosomal dominant 73 MONDO:0957536 TAF4
  10. Intellectual disability, autosomal dominant 22 MONDO:0012869 ZBTB18
  11. Intellectual disability, autosomal dominant 33 MONDO:0014580 DPP6
  12. Intellectual disability, autosomal dominant 34 MONDO:0014599 CERT1
  13. Intellectual disability, autosomal dominant 41 MONDO:0014842 TBL1XR1
  14. Intellectual disability, autosomal dominant 43 MONDO:0014858 HIVEP2
  15. Intellectual disability, autosomal dominant 46 MONDO:0030911 KCNQ5
  16. Intellectual disability, autosomal dominant 47 MONDO:0030912 STAG1
  17. Intellectual disability, autosomal dominant 50 MONDO:0030916 NAA15
  18. Intellectual disability, autosomal dominant 51 MONDO:0030917 KMT5B
  19. Intellectual disability, autosomal dominant 56 MONDO:0030922 CLTC
  20. Intellectual disability, autosomal dominant 57 MONDO:0054837 TLK2
  21. Intellectual disability, autosomal dominant 58 MONDO:0020847 SET
  22. Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language MONDO:0013266 MEF2C

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