4q31.3 - OMIM

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Select item 6124861.

*612486 - DACHSOUS CADHERIN-RELATED 2; DCHS2

CADHERIN J, INCLUDED; CDHJ, INCLUDED

Cytogenetic locations: 15003449

OMIM:: 612486

Gene summaries Genetic tests Medical literature

Select item 6035682.

*603568 - RNA, U73 SMALL NUCLEOLAR; RNU73

OMIM:: 603568

Gene summaries Genetic tests Medical literature

Select item 6116443.

%611644 - HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 9; HSCR9

Cytogenetic locations: 612224

OMIM:: 611644

Gene summaries Genetic tests Medical literature

Select item 6111094.

%611109 - CINNAMON ODOR, PLEASANTNESS OF

Cytogenetic locations: 4q31.3

OMIM:: 611109

Gene summaries Genetic tests Medical literature

Select item 6086745.

*608674 - SH3 DOMAIN PROTEIN 19

SH3D19/RUNX1 FUSION GENE, INCLUDED

Cytogenetic locations: 14551139

OMIM:: 608674

Gene summaries Genetic tests Medical literature

Select item 6114226.

*611422 - MEIOTIC NUCLEAR DIVISIONS 1; MND1

Cytogenetic locations: 11940665

OMIM:: 611422

Gene summaries Genetic tests Medical literature

Select item 6059617.

*605961 - PLEIOTROPIC REGULATOR 1; PLRG1

Cytogenetic locations: 19765207

OMIM:: 605961

Gene summaries Genetic tests Medical literature

Select item 1804788.

*180478 - RIBOSOMAL PROTEIN S3a; RPS3A

Cytogenetic locations: 608000

OMIM:: 180478

Gene summaries Genetic tests Medical literature

Select item 6059289.

*605928 - ADP-RIBOSYLATION FACTOR-INTERACTING PROTEIN 1; ARFIP1

Cytogenetic locations: 10413101

OMIM:: 605928

Gene summaries Genetic tests Medical literature

Select item 24630010.

#246300 - LEPROSY, SUSCEPTIBILITY TO, 3; LPRS3

Cytogenetic locations: 19435236

OMIM:: 246300

Gene summaries Genetic tests Medical literature

Select item 61600411.

#616004 - DYSFIBRINOGENEMIA, CONGENITAL

HYPODYSFIBRINOGENEMIA, CONGENITAL, INCLUDED

Cytogenetic locations: 1p36, 1p36, 1p36

OMIM:: 616004

Gene summaries Genetic tests Medical literature

Select item 61883812.

#618838 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 41; COXPD41

Cytogenetic locations: Smith-McCort

OMIM:: 618838

Gene summaries Genetic tests Medical literature

Select item 61624313.

*616243 - TRANSMEMBRANE PROTEIN 131-LIKE; TMEM131L

Cytogenetic locations: -

OMIM:: 616243

Gene summaries Genetic tests Medical literature

Select item 20240014.

#202400 - AFIBRINOGENEMIA, CONGENITAL

HYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED

Cytogenetic locations: 1p36, 1p36, 1p36

OMIM:: 202400

Gene summaries Genetic tests Medical literature

Select item 62026815.

*620268 - FH2 DOMAIN-CONTAINING PROTEIN 1; FHDC1

Cytogenetic locations: 15138637

OMIM:: 620268

Gene summaries Genetic tests Medical literature

Select item 60415716.

*604157 - SECRETED FRIZZLED-RELATED PROTEIN 2; SFRP2

Cytogenetic locations: mutation

OMIM:: 604157

Gene summaries Genetic tests Medical literature

Select item 62001217.

#620012 - DEVELOPMENTAL DELAY, HYPOTONIA, AND IMPAIRED LANGUAGE; DEDHIL

Cytogenetic locations: 35395208

OMIM:: 620012

Gene summaries Genetic tests Medical literature

Select item 60364518.

*603645 - GLUTAMYL-tRNA AMIDOTRANSFERASE, SUBUNIT B; GATB

Cytogenetic locations: Smith-McCort

OMIM:: 603645

Gene summaries Genetic tests Medical literature

Select item 61549019.

#615490 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R

Cytogenetic locations: Elmod2

OMIM:: 615490

Gene summaries Genetic tests Medical literature

Select item 61587720.

#615877 - MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS

Cytogenetic locations: 24906020

OMIM:: 615877

Gene summaries Genetic tests Medical literature

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