|
FAS
(HGNC:11920)
|
autoimmune lymphoproliferative syndrome type 1
(MONDO_0011158)
|
Definitive
|
|
|
CD40
(HGNC:11919)
|
hyper-IgM syndrome type 3
(MONDO_0011735)
|
Strong
|
|
|
TNFRSF1A
(HGNC:11916)
|
autosomal dominant familial periodic fever
(MONDO_0007727)
|
Definitive
|
|
|
TNFRSF11B
(HGNC:11909)
|
juvenile Paget disease
(MONDO_0009394)
|
Definitive
|
|
|
TNFRSF11A
(HGNC:11908)
|
autosomal recessive osteopetrosis 7
(MONDO_0012859)
|
Limited
|
|
|
TNFRSF11A
(HGNC:11908)
|
osteosarcoma
(MONDO_0009807)
|
Refuted
|
|
|
ACO2
(HGNC:118)
|
optic atrophy 9
(MONDO_0014571)
|
Moderate
|
|
|
TNFRSF11A
(HGNC:11908)
|
dysosteosclerosis
(MONDO_0009138)
|
Moderate
|
|
|
TNFRSF11A
(HGNC:11908)
|
familial expansile osteolysis
(MONDO_0008275)
|
Definitive
|
|
|
ACO2
(HGNC:118)
|
infantile cerebellar-retinal degeneration
(MONDO_0013802)
|
Moderate
|
|
|
TNFAIP3
(HGNC:11896)
|
systemic lupus erythematosus
(MONDO_0007915)
|
Strong
|
|
|
TMPO
(HGNC:11875)
|
dilated cardiomyopathy
(MONDO_0005021)
|
Limited
|
|
|
TLK2
(HGNC:11842)
|
intellectual disability, autosomal dominant 57
(MONDO_0054837)
|
Strong
|
|
|
TKT
(HGNC:11834)
|
transketolase deficiency
(MONDO_0014881)
|
Moderate
|
|
|
TJP2
(HGNC:11828)
|
cholestasis, progressive familial intrahepatic, 4
(MONDO_0014381)
|
Moderate
|
|
|
TK2
(HGNC:11831)
|
mitochondrial disease
(MONDO_0044970)
|
Strong
|
|
|
NKX2-1
(HGNC:11825)
|
hereditary progressive chorea without dementia
(MONDO_0021011)
|
Strong
|
|
|
NKX2-1
(HGNC:11825)
|
brain-lung-thyroid syndrome
(MONDO_0012593)
|
Strong
|
|
|
TINF2
(HGNC:11824)
|
Hoyeraal-Hreidarsson syndrome
(MONDO_0018045)
|
Moderate
|
|
|
TINF2
(HGNC:11824)
|
Revesz syndrome
(MONDO_0009990)
|
Moderate
|
|