About
Site Map
Contact Us
Search
A service of the
U.S. National Library of Medicine®
Home
Conditions
Genes
Chromosomes
Handbook
Glossary
Resources
Genetic Conditions
>
Browse Conditions
1-9
|
A
|
B
|
C
|
D
|
E
|
F
|
G
|
H
|
I
|
J
|
K
|
L
|
M
|
N
|
O
|
P
|
Q-R
|
S
|
T
|
U
|
V
|
W
|
X
|
Y-Z
Kabuki syndrome
Kallmann syndrome
Kanzaki disease
see
Schindler disease
Kast syndrome
see
Maffucci syndrome
Kaufman-McKusick syndrome
see
McKusick-Kaufman syndrome
Kawasaki disease
KD
see
Kawasaki disease
;
spinal and bulbar muscular atrophy
Kearns-Sayre syndrome
Keller syndrome
see
FG syndrome
Kennedy disease
see
spinal and bulbar muscular atrophy
Kennedy spinal and bulbar muscular atrophy
see
spinal and bulbar muscular atrophy
Kerasin histiocytosis
see
Gaucher disease
Kerasin lipoidosis
see
Gaucher disease
Kerasin thesaurismosis
see
Gaucher disease
Keratitis
see
keratitis-ichthyosis-deafness syndrome
keratitis, ichthyosis, and deafness
see
keratitis-ichthyosis-deafness syndrome
keratitis-ichthyosis-deafness syndrome
keratoderma hereditarium mutilans
see
Vohwinkel syndrome
Keratoderma, Palmoplantar
Keratosis Follicularis
see
Darier disease
Ketoacidemia
see
maple syrup urine disease
ketoacidosis due to SCOT deficiency
see
succinyl-CoA:3-ketoacid CoA transferase deficiency
17-ketosteroid reductase deficiency of testis
see
17-beta hydroxysteroid dehydrogenase 3 deficiency
3-Ketothiolase deficiency
see
beta-ketothiolase deficiency
ketotic glycinemia
see
propionic acidemia
ketotic hyperglycinemia
see
propionic acidemia
KFS
see
Klippel-Feil syndrome
KHM
see
Vohwinkel syndrome
KID syndrome
see
keratitis-ichthyosis-deafness syndrome
Kidney Cancer
Kidney Cysts
Kidney Diseases
Kidney Failure
Kidney Stones
see
cystinuria
Kinky Hair Syndrome
see
Menkes syndrome
Kjer type optic atrophy
see
optic atrophy type 1
Kjer's optic atrophy
see
optic atrophy type 1
Kleefstra syndrome
Klinefelter syndrome
Klinefelter's Syndrome
see
Klinefelter syndrome
Klippel-Feil syndrome
Klippel-Trenaunay syndrome
KMS
see
Kabuki syndrome
Kniest dysplasia
Knobloch syndrome
knuckle pads, leukonychia, and sensorineural deafness
see
Bart-Pumphrey syndrome
Koolen-De Vries syndrome
see
17q21.31 microdeletion syndrome
Koolen syndrome
see
17q21.31 microdeletion syndrome
Kostmann disease
see
severe congenital neutropenia
Kostmann's agranulocytosis
see
severe congenital neutropenia
Kostmann's syndrome
see
severe congenital neutropenia
Krabbe disease
Krause-Kivlin syndrome
see
Peters plus syndrome
Krause-van Schooneveld-Kivlin syndrome
see
Peters plus syndrome
17-KSR deficiency
see
17-beta hydroxysteroid dehydrogenase 3 deficiency
KSS
see
Kearns-Sayre syndrome
KTS
see
Klippel-Trenaunay syndrome
KTW syndrome
see
Klippel-Trenaunay syndrome
Kufs disease
Kymenlaakso syndrome
see
lattice corneal dystrophy type II
Published: February 11, 2013