|
TINF2
(HGNC:11824)
|
thyroid gland papillary carcinoma
(MONDO_0005075)
|
Limited
|
|
|
TINF2
(HGNC:11824)
|
pulmonary fibrosis
(MONDO_0002771)
|
Limited
|
|
|
MYRF
(HGNC:1181)
|
cardiac-urogenital syndrome
(MONDO_0032653)
|
Strong
|
|
|
MYRF
(HGNC:1181)
|
encephalitis/encephalopathy, mild, with reversible myelin vacuolization
(MONDO_0020853)
|
Moderate
|
|
|
TIMM8A
(HGNC:11817)
|
deafness dystonia syndrome
(MONDO_0010578)
|
Strong
|
|
|
KLF11
(HGNC:11811)
|
maturity-onset diabetes of the young
(MONDO_0018911)
|
Limited
|
|
|
KLF11
(HGNC:11811)
|
monogenic diabetes
(MONDO_0015967)
|
Limited
|
|
|
KLF11
(HGNC:11811)
|
maturity-onset diabetes of the young type 7
(MONDO_0012513)
|
Limited
|
|
|
KLF10
(HGNC:11810)
|
hypertrophic cardiomyopathy
(MONDO_0005045)
|
Limited
|
|
|
TIA1
(HGNC:11802)
|
distal myopathy, Welander type
(MONDO_0011466)
|
Strong
|
|
|
TH
(HGNC:11782)
|
tyrosine hydroxylase deficiency
(MONDO_0100064)
|
Definitive
|
|
|
THPO
(HGNC:11795)
|
congenital amegakaryocytic thrombocytopenia
(MONDO_0800451)
|
Strong
|
|
|
THPO
(HGNC:11795)
|
familial thrombocytosis
(MONDO_0019111)
|
Strong
|
|
|
TH
(HGNC:11782)
|
TH-deficient dopa-responsive dystonia
(MONDO_0011551)
|
Strong
|
|
|
TGM1
(HGNC:11777)
|
congenital non-bullous ichthyosiform erythroderma
(MONDO_0019306)
|
Strong
|
|
|
TGM1
(HGNC:11777)
|
acral self-healing collodion baby
(MONDO_0017268)
|
Limited
|
|
|
TGM1
(HGNC:11777)
|
self-healing collodion baby
(MONDO_0017267)
|
Moderate
|
|
|
TGM1
(HGNC:11777)
|
bathing suit ichthyosis
(MONDO_0015085)
|
Strong
|
|
|
TGFBR2
(HGNC:11773)
|
Loeys-Dietz syndrome
(MONDO_0018954)
|
Definitive
|
|
|
TGFBR1
(HGNC:11772)
|
Loeys-Dietz syndrome
(MONDO_0018954)
|
Definitive
|
|