Prematurity or preterm - OMIM - NCBI

Prematurity or preterm - OMIM - NCBI



From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

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• Search OMIM for "Prematurity or preterm" 

#608649 - ICHTHYOSIS PREMATURITY SYNDROME; IPS

Cytogenetic locations: 9q34.11

OMIM:

 

608649

Gene summaries Genetic tests Medical literature

Select item 2674502.

267450 - RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS

OMIM:

 

267450

Gene summaries Genetic tests Medical literature

Select item 1337803.

#133780 - EXUDATIVE VITREORETINOPATHY 1; EVR1

RETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED

Cytogenetic locations: 11q14.2

OMIM:

 

133780

Gene summaries Genetic tests Medical literature

Select item 6105044.

#610504 - PRETERM PREMATURE RUPTURE OF THE MEMBRANES; PPROM

Cytogenetic locations: 11q13.5

OMIM:

 

610504

Gene summaries Genetic tests Medical literature

Select item 6041945.

*604194 - SOLUTE CARRIER FAMILY 27 (FATTY ACID TRANSPORTER), MEMBER 4; SLC27A4

Cytogenetic locations: 9q34.11

OMIM:

 

604194

Gene summaries Genetic tests Medical literature

Select item 6045796.

*604579 - FRIZZLED, DROSOPHILA, HOMOLOG OF, 4; FZD4

Cytogenetic locations: 11q14.2

OMIM:

 

604579

Gene summaries Genetic tests Medical literature

Select item 6009437.

*600943 - SERPIN PEPTIDASE INHIBITOR, CLADE H, MEMBER 1; SERPINH1

CBP1, INCLUDED

Cytogenetic locations: 11q13.5

OMIM:

 

600943

Gene summaries Genetic tests Medical literature

Select item 3009718.

#300971 - BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT; BARTS5

Cytogenetic locations: Xp11.21

OMIM:

 

300971

Gene summaries Genetic tests Medical literature

Select item 2180409.

#218040 - COSTELLO SYNDROME; CSTLO

MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES, INCLUDED; CMEMS, INCLUDED

Cytogenetic locations: 11p15.5

OMIM:

 

218040

Gene summaries Genetic tests Medical literature

Select item 24519010.

245190 - KNIEST-LIKE DYSPLASIA, LETHAL

OMIM:

 

245190

Gene summaries Genetic tests Medical literature

Select item 61254011.

#612540 - MYOPATHY, CONGENITAL, COMPTON-NORTH; MYPCN

Cytogenetic locations: 12q12

OMIM:

 

612540

Gene summaries Genetic tests Medical literature

Select item 25630012.

#256300 - NEPHROTIC SYNDROME, TYPE 1; NPHS1

Cytogenetic locations: 19q13.12

OMIM:

 

256300

Gene summaries Genetic tests Medical literature

Select item 61705313.

#617053 - MIRAGE SYNDROME; MIRAGE

Cytogenetic locations: 7q21.2

OMIM:

 

617053

Gene summaries Genetic tests Medical literature

Select item 61665114.

#616651 - ROIFMAN SYNDROME; RFMN

Cytogenetic locations: 2q14.2

OMIM:

 

616651

Gene summaries Genetic tests Medical literature

Select item 61009015.

#610090 - PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY; PNPOD

Cytogenetic locations: 17q21.32

OMIM:

 

610090

Gene summaries Genetic tests Medical literature

Select item 21634016.

#216340 - YUNIS-VARON SYNDROME; YVS

Cytogenetic locations: 6q21

OMIM:

 

216340

Gene summaries Genetic tests Medical literature

Select item 12035517.

*120355 - MATRIX METALLOPROTEINASE 8; MMP8

Cytogenetic locations: 11q22.2

OMIM:

 

120355

Gene summaries Genetic tests Medical literature

Select item 12035318.

*120353 - MATRIX METALLOPROTEINASE 1; MMP1

Cytogenetic locations: 11q22.2

OMIM:

 

120353

Gene summaries Genetic tests Medical literature

Select item 17982019.

*179820 - RENIN; REN

Cytogenetic locations: 1q32.1

OMIM:

 

179820

Gene summaries Genetic tests Medical literature

Select item 60026220.

*600262 - PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 2; PTGS2

Cytogenetic locations: 1q31.1

OMIM:

 

600262

Gene summaries Genetic tests Medical literature