|
OMIM |
Link |
Information gain |
01 |
|
deafness, congenital, and onychodystrophy, recessive form
|
[NCBI]
|
0.00782442
|
|
|
coffin-siris syndrome
|
[NCBI]
|
0.00689527
|
|
|
onychotrichodysplasia and neutropenia
|
[NCBI]
|
0.00205655
|
|
|
ZLS
|
[NCBI]
|
0.00135668
|
|
|
anonychia-onychodystrophy with hypoplasia or absence of distal phalanges
|
[NCBI]
|
0.00130408
|
|
|
ectodermal dysplasia, absent dermatoglyphic pattern, changes in nails, and simian crease
|
[NCBI]
|
0.00130408
|
|
|
koilonychia, hereditary
|
[NCBI]
|
0.00116933
|
|
|
leukonychia totalis
|
[NCBI]
|
0.00100669
|
|
|
schopf-schulz-passarge syndrome
|
[NCBI]
|
0.00090173
|
|
|
brachydactyly, type a5, with nail dysplasia
|
[NCBI]
|
0.000800285
|
|
|
coloboma of macula
|
[NCBI]
|
0.000800285
|
|
|
triphalangeal thumb, nonopposable
|
[NCBI]
|
0.000800285
|
|
|
curly hair-acral keratoderma-caries syndrome
|
[NCBI]
|
0.000800285
|
|
|
PC1
|
[NCBI]
|
0.000693866
|
|
|
anonychia congenita
|
[NCBI]
|
0.000589259
|
|
|
otoonychoperoneal syndrome
|
[NCBI]
|
0.000583287
|
|
|
nail dysplasia
|
[NCBI]
|
0.000583287
|
|
|
NPS
|
[NCBI]
|
0.000523618
|
|
|
symphalangism, distal
|
[NCBI]
|
0.000501982
|
|
|
dermal ridges, patternless
|
[NCBI]
|
0.000501982
|
|
|
sabinas brittle hair syndrome
|
[NCBI]
|
0.000501982
|
|
|
FRNS
|
[NCBI]
|
0.0004746
|
|
|
DKC
|
[NCBI]
|
0.00044224
|
|
|
PC2
|
[NCBI]
|
0.000429364
|
|
|
AOS
|
[NCBI]
|
0.000383886
|
|
|
epiphyseal dysplasia, microcephaly, and nystagmus
|
[NCBI]
|
0.000380062
|
|
|
witkop syndrome
|
[NCBI]
|
0.000361483
|
|
|
hypertelorism, teebi type
|
[NCBI]
|
0.000354699
|
|
|
sclerotylosis
|
[NCBI]
|
0.000354699
|
|
|
epidermolysis bullosa with congenital localized absence of skin and deformity of nails
|
[NCBI]
|
0.000345923
|
|
|
arthrogryposis and ectodermal dysplasia
|
[NCBI]
|
0.000317322
|
|
|
RA
|
[NCBI]
|
0.000299009
|
|
|
OODD
|
[NCBI]
|
0.000280882
|
|
|
PURE&apos
|
[NCBI]
|
0.000262819
|
|
|
RSPO4
|
[NCBI]
|
0.000259075
|
|
|
nail dysplasia, isolated congenital
|
[NCBI]
|
0.000236716
|
|
|
COL7A1
|
[NCBI]
|
0.000212154
|
|
|
KRT16
|
[NCBI]
|
0.000211561
|
|
|
ectodermal dysplasia, trichoodontoonychial type
|
[NCBI]
|
0.000211424
|
|
|
curved nail of fourth toe
|
[NCBI]
|
0.000211424
|
|
|
tonoki syndrome
|
[NCBI]
|
0.000211424
|
|
|
SLE
|
[NCBI]
|
0.000211297
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
0.000194362
|
|
|
KRT17
|
[NCBI]
|
0.000192009
|
|
|
ROR2
|
[NCBI]
|
0.00018234
|
|
|
brachymorphism-onychodysplasia-dysphalangism syndrome
|
[NCBI]
|
0.000180493
|
|
|
hearing loss, sensorineural, with enamel hypoplasia and nail defects
|
[NCBI]
|
0.000166526
|
|
|
yellow nail syndrome
|
[NCBI]
|
0.000156945
|
|
|
weyers acrofacial dysostosis
|
[NCBI]
|
0.000149609
|
|
|
steatocystoma multiplex
|
[NCBI]
|
0.000149609
|
|
|
FDH
|
[NCBI]
|
0.000139639
|
|
|
monilethrix
|
[NCBI]
|
0.000130495
|
|
|
anonychia-ectrodactyly
|
[NCBI]
|
0.00010565
|
|
|
anonychia-onychodystrophy
|
[NCBI]
|
0.00010565
|
|
|
trichoodontoonychial dysplasia
|
[NCBI]
|
0.00010565
|
|
|
anonychia, total, with microcephaly
|
[NCBI]
|
0.00010565
|
|
|
endothelial dystrophy, congenital hereditary, with nail hypoplasia
|
[NCBI]
|
0.00010565
|
|
|
anonychia-onychodystrophy with brachydactyly type b and ectrodactyly
|
[NCBI]
|
0.00010565
|
|
|
ectodermal dysplasia with adrenal cyst
|
[NCBI]
|
0.00010565
|
|
|
hirschsprung disease with hypoplastic nails and dysmorphic facial features
|
[NCBI]
|
0.00010565
|
|
|
corneodermatoosseous syndrome
|
[NCBI]
|
0.00010565
|
|
|
odontotrichoungual-digital-palmar syndrome
|
[NCBI]
|
0.00010565
|
|
|
anonychia with flexural pigmentation
|
[NCBI]
|
0.00010565
|
|
|
ulnar hypoplasia with mental retardation
|
[NCBI]
|
0.00010565
|
|
|
ectodermal dysplasia, hidrotic, christianson-fourie type
|
[NCBI]
|
0.00010565
|
|
|
hirschsprung disease with type d brachydactyly
|
[NCBI]
|
0.00010565
|
|
|
sella turcica, bridged
|
[NCBI]
|
0.00010565
|
|
|
onycholysis, partial, with scleronychia
|
[NCBI]
|
0.00010565
|
|
|
CFNS
|
[NCBI]
|
9.29736e-05
|
|
|
WNT10A
|
[NCBI]
|
8.5955e-05
|
|
|
KRN1
|
[NCBI]
|
8.5955e-05
|
|
|
trigonocephaly with short stature and developmental delay
|
[NCBI]
|
8.32014e-05
|
|
|
dermoodontodysplasia
|
[NCBI]
|
8.32014e-05
|
|
|
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities
|
[NCBI]
|
8.32014e-05
|
|
|
pachyonychia congenita, recessive
|
[NCBI]
|
7.47431e-05
|
|
|
chands
|
[NCBI]
|
7.47431e-05
|
|
|
toenail dystrophy, isolated
|
[NCBI]
|
7.47431e-05
|
|
|
keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy
|
[NCBI]
|
7.47431e-05
|
|
|
LOCS
|
[NCBI]
|
6.92586e-05
|
|
|
epidermolysis bullosa, late-onset localized junctional, with mental retardation
|
[NCBI]
|
6.92586e-05
|
|
|
coloboma of macula with type b brachydactyly
|
[NCBI]
|
6.92586e-05
|
|
|
carbimazole sensitivity
|
[NCBI]
|
6.92586e-05
|
|
|
dyskeratosis congenita, autosomal recessive
|
[NCBI]
|
6.92586e-05
|
|
|
polyposis, skin pigmentation, alopecia, and fingernail changes
|
[NCBI]
|
6.92586e-05
|
|
|
kabuki syndrome
|
[NCBI]
|
6.85218e-05
|
|
|
FOXN1
|
[NCBI]
|
6.69762e-05
|
|
|
ED3
|
[NCBI]
|
6.51865e-05
|
|
|
knuckle pads, leukonychia, and sensorineural deafness
|
[NCBI]
|
6.51865e-05
|
|
|
scalp-ear-nipple syndrome
|
[NCBI]
|
6.51865e-05
|
|
|
KRT6A
|
[NCBI]
|
6.36001e-05
|
|
|
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly
|
[NCBI]
|
6.19463e-05
|
|
|
frontonasal dysplasia
|
[NCBI]
|
5.69559e-05
|
|
|
BDB1
|
[NCBI]
|
5.31672e-05
|
|
|
lymphedema, hereditary, ii
|
[NCBI]
|
5.31672e-05
|
|
|
KRT10
|
[NCBI]
|
5.26608e-05
|
|
|
adult syndrome
|
[NCBI]
|
4.87868e-05
|
|
|
SYNS1
|
[NCBI]
|
4.87868e-05
|
|
|
lymphedema, hereditary, i
|
[NCBI]
|
4.87868e-05
|
|
|
MSX1
|
[NCBI]
|
4.81758e-05
|
|
|
indifference to pain, congenital, autosomal recessive
|
[NCBI]
|
4.75625e-05
|
|
|
LMS
|
[NCBI]
|
4.64275e-05
|
|
|
IP
|
[NCBI]
|
4.54029e-05
|
|
|
epidermolysis bullosa simplex and limb-girdle muscular dystrophy
|
[NCBI]
|
4.438e-05
|
|
|
DRRS
|
[NCBI]
|
4.34497e-05
|
|
|
ED2
|
[NCBI]
|
4.34497e-05
|
|
|
COL17A1
|
[NCBI]
|
4.20915e-05
|
|
|
RHS
|
[NCBI]
|
4.09559e-05
|
|
|
robinow syndrome, autosomal recessive
|
[NCBI]
|
4.02075e-05
|
|
|
GABEB
|
[NCBI]
|
3.94943e-05
|
|
|
weaver syndrome
|
[NCBI]
|
3.88132e-05
|
|
|
PPS
|
[NCBI]
|
3.81614e-05
|
|
|
HMI
|
[NCBI]
|
3.81408e-05
|
|
|
epidermolysis bullosa letalis
|
[NCBI]
|
3.58051e-05
|
|
|
leopard syndrome 1
|
[NCBI]
|
3.47533e-05
|
|
|
CDPX2
|
[NCBI]
|
3.19853e-05
|
|
|
charge syndrome
|
[NCBI]
|
3.1571e-05
|
|
|
EVC
|
[NCBI]
|
3.11682e-05
|
|
|
exostoses, multiple, type i
|
[NCBI]
|
3.07764e-05
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
3.0395e-05
|
|
|
PHS
|
[NCBI]
|
2.93082e-05
|
|
|
CMTC
|
[NCBI]
|
2.86273e-05
|
|
|
HGPS
|
[NCBI]
|
2.11346e-05
|
|
|
AHO
|
[NCBI]
|
1.72336e-05
|
|
|
WBS
|
[NCBI]
|
8.40602e-06
|
|