Human | LHX4 | 89884 | LIM homeobox 4 |
HP RolledUp, OMIM ID: 262700 Category = humanphenotype |
Human | AAAS | 8086 | achalasia, adrenocortical insufficiency, alacrimia |
HP RolledUp, OMIM ID: 231550 Category = humanphenotype |
Human | LHX3 | 8022 | LIM homeobox 3 |
HP RolledUp, OMIM ID: 262600 Category = humanphenotype |
Human | BSND | 7809 | Bartter syndrome, infantile, with sensorineural deafness (Barttin) |
HP RolledUp, OMIM ID: 602522 Category = humanphenotype |
Human | SLC12A1 | 6557 | solute carrier family 12 (sodium/potassium/chloride transporter), member 1 |
HP RolledUp, OMIM ID: 601678 Category = humanphenotype |
Human | SCNN1G | 6340 | sodium channel, non-voltage-gated 1, gamma subunit |
HP RolledUp, OMIM ID: 264350 Category = humanphenotype
HP RolledUp, OMIM ID: 177200 Category = humanphenotype |
Human | SCNN1B | 6338 | sodium channel, non-voltage-gated 1, beta subunit |
HP RolledUp, OMIM ID: 264350 Category = humanphenotype
HP RolledUp, OMIM ID: 177200 Category = humanphenotype |
Human | SCNN1A | 6337 | sodium channel, non-voltage-gated 1 alpha subunit |
HP RolledUp, OMIM ID: 264350 Category = humanphenotype |
Human | PROP1 | 5626 | PROP paired-like homeobox 1 |
HP RolledUp, OMIM ID: 262600 Category = humanphenotype |
Human | POU1F1 | 5449 | POU class 1 homeobox 1 |
HP RolledUp, OMIM ID: 262600 Category = humanphenotype |
Human | OCRL | 4952 | oculocerebrorenal syndrome of Lowe |
HP RolledUp, OMIM ID: 309000 Category = humanphenotype |
Human | NR3C2 | 4306 | nuclear receptor subfamily 3, group C, member 2 |
HP RolledUp, OMIM ID: 177735 Category = humanphenotype |
Human | KCNJ10 | 3766 | potassium inwardly-rectifying channel, subfamily J, member 10 |
HP RolledUp, OMIM ID: 612780 Category = humanphenotype |
Human | KCNJ5 | 3762 | potassium inwardly-rectifying channel, subfamily J, member 5 |
HP RolledUp, OMIM ID: 613677 Category = humanphenotype |
Human | KCNJ1 | 3758 | potassium inwardly-rectifying channel, subfamily J, member 1 |
HP RolledUp, OMIM ID: 241200 Category = humanphenotype |
Human | HSD11B2 | 3291 | hydroxysteroid (11-beta) dehydrogenase 2 |
HP RolledUp, OMIM ID: 218030 Category = humanphenotype |
Human | SLC26A3 | 1811 | solute carrier family 26 (anion exchanger), member 3 |
HP RolledUp, OMIM ID: 214700 Category = humanphenotype |
Human | CYP11B2 | 1585 | cytochrome P450, family 11, subfamily B, polypeptide 2 |
HP RolledUp, OMIM ID: 124080 Category = humanphenotype
HP RolledUp, OMIM ID: 610600 Category = humanphenotype
HP RolledUp, OMIM ID: 203400 Category = humanphenotype |
Human | CYP11B1 | 1584 | cytochrome P450, family 11, subfamily B, polypeptide 1 |
HP RolledUp, OMIM ID: 103900 Category = humanphenotype |
Human | CYP11A1 | 1583 | cytochrome P450, family 11, subfamily A, polypeptide 1 |
HP RolledUp, OMIM ID: 613743 Category = humanphenotype |
Human | CLCNKB | 1188 | chloride channel, voltage-sensitive Kb |
HP RolledUp, OMIM ID: 613090 Category = humanphenotype
HP RolledUp, OMIM ID: 607364 Category = humanphenotype
HP RolledUp, OMIM ID: 602522 Category = humanphenotype |
Human | CLCNKA | 1187 | chloride channel, voltage-sensitive Ka |
HP RolledUp, OMIM ID: 602522 Category = humanphenotype
HP RolledUp, OMIM ID: 613090 Category = humanphenotype |
Human | AIRE | 326 | autoimmune regulator |
HP RolledUp, OMIM ID: 240300 Category = humanphenotype |
Human | NR0B1 | 190 | nuclear receptor subfamily 0, group B, member 1 |
HP RolledUp, OMIM ID: 300200 Category = humanphenotype |