17p12 - OMIM

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Select item 6133921.

%613392 - DEAFNESS, AUTOSOMAL RECESSIVE 85; DFNB85

Cytogenetic locations: 17p13.2

OMIM:: 613392

Gene summaries Genetic tests Medical literature

Select item 1366602.

#136660 - FRAGILE SITE 17p12

OMIM:: 136660

Gene summaries Genetic tests Medical literature

Select item 6055723.

%605572 - ABDOMINAL OBESITY-METABOLIC SYNDROME QUANTITATIVE TRAIT LOCUS 2

Cytogenetic locations: 11121050

OMIM:: 605572

Gene summaries Genetic tests Medical literature

Select item 6173274.

*617327 - SHISA FAMILY, MEMBER 6; SHISA6

Cytogenetic locations: P2RX1

OMIM:: 617327

Gene summaries Genetic tests Medical literature

Select item 1945245.

*194524 - ZINC FINGER PROTEIN 18; ZNF18

Cytogenetic locations: possible

OMIM:: 194524

Gene summaries Genetic tests Medical literature

Select item 1945356.

*194535 - ZINC FINGER PROTEIN 29, PSEUDOGENE; ZNF29P

Cytogenetic locations: p2004757

OMIM:: 194535

Gene summaries Genetic tests Medical literature

Select item 6149287.

%614928 - ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE; ECTD6

Cytogenetic locations: 17107387

OMIM:: 614928

Gene summaries Genetic tests Medical literature

Select item 6040588.

*604058 - HEPARAN SULFATE-GLUCOSAMINE 3-SULFOTRANSFERASE 3B1; HS3ST3B1

OMIM:: 604058

Gene summaries Genetic tests Medical literature

Select item 6045969.

*604596 - F-BOX AND WD REPEAT DOMAIN 10B; FBXW10B

Cytogenetic locations: 609426

OMIM:: 604596

Gene summaries Genetic tests Medical literature

Select item 61871910.

#618719 - MEGABLADDER, CONGENITAL; MGBL

Cytogenetic locations: 31513549

OMIM:: 618719

Gene summaries Genetic tests Medical literature

Select item 60405711.

*604057 - HEPARAN SULFATE-GLUCOSAMINE 3-SULFOTRANSFERASE 3A1; HS3ST3A1

Cytogenetic locations: 609455

OMIM:: 604057

Gene summaries Genetic tests Medical literature

Select item 61206812.

*612068 - PHOSPHOINOSITIDE-INTERACTING REGULATOR OF TRANSIENT RECEPTOR POTENTIAL CHANNELS; PIRT

Cytogenetic locations: 18455988

OMIM:: 612068

Gene summaries Genetic tests Medical literature

Select item 61665213.

#616652 - YUAN-HAREL-LUPSKI SYNDROME; YUHAL

Cytogenetic locations: 26544804

OMIM:: 616652

Gene summaries Genetic tests Medical literature

Select item 61983414.

#619834 - OVARIAN DYSGENESIS 10; ODG10

Cytogenetic locations: 34402903

OMIM:: 619834

Gene summaries Genetic tests Medical literature

Select item 61771615.

*617716 - RHO GTPase-ACTIVATING PROTEIN 44; ARHGAP44

Cytogenetic locations: Ube2g1

OMIM:: 617716

Gene summaries Genetic tests Medical literature

Select item 61544016.

#615440 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17; COXPD17

Cytogenetic locations: 23849775

OMIM:: 615440

Gene summaries Genetic tests Medical literature

Select item 61983117.

#619831 - SPERMATOGENIC FAILURE 71; SPGF71

Cytogenetic locations: 33713115

OMIM:: 619831

Gene summaries Genetic tests Medical literature

Select item 62027718.

#620277 - SPERMATOGENIC FAILURE 81; SPGF81

Cytogenetic locations: 604657

OMIM:: 620277

Gene summaries Genetic tests Medical literature

Select item 11830019.

#118300 - CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS

Cytogenetic locations: 605398

OMIM:: 118300

Gene summaries Genetic tests Medical literature

Select item 18080020.

#180800 - ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA

Cytogenetic locations: 1p36, 1p36

OMIM:: 180800

Gene summaries Genetic tests Medical literature

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