|
LSS
(HGNC:6708)
|
hypotrichosis simplex
(MONDO_0018914)
|
Moderate
|
|
|
LRRFIP1
(HGNC:6702)
|
schizophrenia
(MONDO_0005090)
|
Limited
|
|
|
LRP6
(HGNC:6698)
|
tooth agenesis
(MONDO_0005486)
|
Strong
|
|
|
LRP5
(HGNC:6697)
|
exudative vitreoretinopathy
(MONDO_0019516)
|
Definitive
|
|
|
LRP5
(HGNC:6697)
|
osteoporosis-pseudoglioma syndrome
(MONDO_0009820)
|
Definitive
|
|
|
LRP5
(HGNC:6697)
|
hyperostosis corticalis generalisata
(MONDO_0009395)
|
Moderate
|
|
|
LRP5
(HGNC:6697)
|
autosomal dominant osteosclerosis, Worth type
(MONDO_0007764)
|
Strong
|
|
|
LRP4
(HGNC:6696)
|
sclerosteosis
(MONDO_0017838)
|
Moderate
|
|
|
LRP4
(HGNC:6696)
|
congenital myasthenic syndrome 17
(MONDO_0014578)
|
Moderate
|
|
|
LRP4
(HGNC:6696)
|
sclerosteosis 2
(MONDO_0013679)
|
Moderate
|
|
|
LRP2
(HGNC:6694)
|
Stickler syndrome
(MONDO_0019354)
|
Limited
|
|
|
LRP1
(HGNC:6692)
|
schizophrenia
(MONDO_0005090)
|
Limited
|
|
|
LRAT
(HGNC:6685)
|
retinitis pigmentosa
(MONDO_0019200)
|
Moderate
|
|
|
LRAT
(HGNC:6685)
|
Leber congenital amaurosis
(MONDO_0018998)
|
Strong
|
|
|
RHOA
(HGNC:667)
|
ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies
(MONDO_0032884)
|
Limited
|
|
|
LRAT
(HGNC:6685)
|
severe early-childhood-onset retinal dystrophy
(MONDO_0009549)
|
Strong
|
|
|
LPL
(HGNC:6677)
|
hyperlipidemia, familial combined, LPL related
(MONDO_0007759)
|
Limited
|
|
|
LORICRIN
(HGNC:6663)
|
loricrin keratoderma
(MONDO_0011396)
|
Strong
|
|
|
LMX1B
(HGNC:6654)
|
nail-patella-like renal disease
(MONDO_0009724)
|
Moderate
|
|
|
LMX1B
(HGNC:6654)
|
nail-patella syndrome
(MONDO_0008061)
|
Definitive
|
|