Related Entries for OMIM (Select 607872) - OMIM - NCBI

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Select item 6078721.

#607872 - CHROMOSOME 1p36 DELETION SYNDROME, DISTAL

Cytogenetic locations: 1p36

OMIM:: 607872

Gene summaries Genetic tests Medical literature

Select item 6193432.

#619343 - CHROMOSOME 1p36 DELETION SYNDROME, PROXIMAL

Cytogenetic locations: 1p36

OMIM:: 619343

Gene summaries Genetic tests Medical literature

Select item 6193123.

#619312 - RADIO-TARTAGLIA SYNDROME; RATARS

Cytogenetic locations: 1p36.21-p36.13

OMIM:: 619312

Gene summaries Genetic tests Medical literature

Select item 6169754.

#616975 - NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART; NEDBEH

Cytogenetic locations: 1p36.23

OMIM:: 616975

Gene summaries Genetic tests Medical literature

Select item 6167895.

#616789 - IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD

Cytogenetic locations: 619253

OMIM:: 616789

Gene summaries Genetic tests Medical literature

Select item 6153736.

#615373 - LEFT VENTRICULAR NONCOMPACTION 8; LVNC8

CARDIOMYOPATHY, DILATED, 1LL, INCLUDED; CMD1LL, INCLUDED

Cytogenetic locations: 1p36.32

OMIM:: 615373

Gene summaries Genetic tests Medical literature

Select item 6134847.

*613484 - SPEN FAMILY TRANSCRIPTIONAL REPRESSOR; SPEN

Cytogenetic locations: 1p36.21-p36.13

OMIM:: 613484

Gene summaries Genetic tests Medical literature

Select item 6107718.

*610771 - CHROMODOMAIN HELICASE DNA-BINDING PROTEIN 5; CHD5

Cytogenetic locations: 1p36.31

OMIM:: 610771

Gene summaries Genetic tests Medical literature

Select item 6062429.

%606242 - KONDOH SYNDROME

Cytogenetic locations: 1p36.32-p35.3

OMIM:: 606242

Gene summaries Genetic tests Medical literature

Select item 60555710.

*605557 - PR DOMAIN-CONTAINING PROTEIN 16; PRDM16

Cytogenetic locations: 1p36.32

OMIM:: 605557

Gene summaries Genetic tests Medical literature

Select item 60522611.

*605226 - ARGININE-GLUTAMIC ACID DIPEPTIDE REPEATS; RERE

Cytogenetic locations: 1p36.23

OMIM:: 605226

Gene summaries Genetic tests Medical literature

Select item 60416912.

#604169 - LEFT VENTRICULAR NONCOMPACTION 1; LVNC1

Cytogenetic locations: 12372586

OMIM:: 604169

Gene summaries Genetic tests Medical literature

Select item 60373613.

#603736 - OHDO SYNDROME, SBBYS VARIANT; SBBYSS

Cytogenetic locations: 33430551

OMIM:: 603736

Gene summaries Genetic tests Medical literature

Select item 60136514.

*601365 - DISHEVELLED 1; DVL1

Cytogenetic locations: 1p36.33

OMIM:: 601365

Gene summaries Genetic tests Medical literature

Select item 60114215.

*601142 - POTASSIUM CHANNEL, VOLTAGE-GATED, SHAKER-RELATED SUBFAMILY, BETA MEMBER 2; KCNAB2

Cytogenetic locations: 1p36.31

OMIM:: 601142

Gene summaries Genetic tests Medical literature

Select item 60011816.

#600118 - WARBURG MICRO SYNDROME 1; WARBM1

Cytogenetic locations: 17351351

OMIM:: 600118

Gene summaries Genetic tests Medical literature

Select item 30405017.

%304050 - AICARDI SYNDROME; AIC

Cytogenetic locations: 14061784

OMIM:: 304050

Gene summaries Genetic tests Medical literature

Select item 30004918.

#300049 - PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1

HETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA, INCLUDED

OMIM:: 300049

Gene summaries Genetic tests Medical literature

Select item 30001719.

*300017 - FILAMIN A; FLNA

Cytogenetic locations: 14988809

OMIM:: 300017

Gene summaries Genetic tests Medical literature

Select item 25804020.

258040 - OEIS COMPLEX

OMIM:: 258040

Gene summaries Genetic tests Medical literature

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