OMIM Links for Nucleotide (Select 1890253844) - OMIM

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Links from Nucleotide

Items: 1 to 20 of 31

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Select item 6198771.

#619877 - DENTICI-NOVELLI NEURODEVELOPMENTAL SYNDROME; DENNED

Cytogenetic locations: 21937992

OMIM:: 619877

Gene summaries Genetic tests Medical literature

Select item 6191812.

*619181 - FAMILY WITH SEQUENCE SIMILARITY 177, MEMBER A1; FAM177A1

Cytogenetic locations: 19663910

OMIM:: 619181

Gene summaries Genetic tests Medical literature

Select item 6188903.

#618890 - NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY; NEDBASS

Cytogenetic locations: 612007

OMIM:: 618890

Gene summaries Genetic tests Medical literature

Select item 6185484.

#618548 - MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 4; MCAHS4

Cytogenetic locations: 31148362

OMIM:: 618548

Gene summaries Genetic tests Medical literature

Select item 6183485.

#618348 - GALLOWAY-MOWAT SYNDROME 7; GAMOS7

Cytogenetic locations: 28280135

OMIM:: 618348

Gene summaries Genetic tests Medical literature

Select item 6182216.

#618221 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 66; MRT66

Cytogenetic locations: MCAM

OMIM:: 618221

Gene summaries Genetic tests Medical literature

Select item 6179137.

#617913 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR

Cytogenetic locations: 27878435

OMIM:: 617913

Gene summaries Genetic tests Medical literature

Select item 6178358.

*617835 - PYRUVATE DEHYDROGENASE PHOSPHATASE REGULATORY SUBUNIT; PDPR

Cytogenetic locations: 12056414

OMIM:: 617835

Gene summaries Genetic tests Medical literature

Select item 6178229.

#617822 - ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS

Cytogenetic locations: 19640479

OMIM:: 617822

Gene summaries Genetic tests Medical literature

Select item 61712610.

#617126 - ALAZAMI-YUAN SYNDROME; ALYUS

Cytogenetic locations: 25574841

OMIM:: 617126

Gene summaries Genetic tests Medical literature

Select item 61702611.

#617026 - PONTOCEREBELLAR HYPOPLASIA, TYPE 2F; PCH2F

Cytogenetic locations: 27392077

OMIM:: 617026

Gene summaries Genetic tests Medical literature

Select item 61702012.

#617020 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 38; DEE38

Cytogenetic locations: 27270415

OMIM:: 617020

Gene summaries Genetic tests Medical literature

Select item 61690113.

#616901 - DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR 1; DEDSSH1

Cytogenetic locations: 30877278

OMIM:: 616901

Gene summaries Genetic tests Medical literature

Select item 61690014.

#616900 - HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3; IHPRF3

Cytogenetic locations: 27040692

OMIM:: 616900

Gene summaries Genetic tests Medical literature

Select item 61689915.

*616899 - TBC1 DOMAIN-CONTAINING KINASE; TBCK

Cytogenetic locations: 24576458

OMIM:: 616899

Gene summaries Genetic tests Medical literature

Select item 61626316.

#616263 - NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 1; IMNEPD1

Cytogenetic locations: 28328138

OMIM:: 616263

Gene summaries Genetic tests Medical literature

Select item 61608217.

*616082 - CHROMOSOME 12 OPEN READING FRAME 4; C12ORF4

Cytogenetic locations: MCAM

OMIM:: 616082

Gene summaries Genetic tests Medical literature

Select item 61438718.

*614387 - ZINC FINGER PROTEIN 526; ZNF526

Cytogenetic locations: 21937992

OMIM:: 614387

Gene summaries Genetic tests Medical literature

Select item 61421819.

*614218 - WD REPEAT-CONTAINING PROTEIN 81; WDR81

Cytogenetic locations: 16371500

OMIM:: 614218

Gene summaries Genetic tests Medical literature

Select item 61164720.

*611647 - ARV1 HOMOLOG, FATTY ACID HOMEOSTASIS MODULATOR; ARV1

Cytogenetic locations: 11063737

OMIM:: 611647

Gene summaries Genetic tests Medical literature

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OMIM Links for Nucleotide (Select 1890253844) (31)
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Chromosome neighbors for GEO Profiles (Select 117494277) (20)
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Profile neighbors for GEO Profiles (Select 1013177) (36)
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OMIM Links for GEO Profiles (Select 34579350) (1)
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KLK12 kallikrein related peptidase 12 [Homo sapiens]
KLK12 kallikrein related peptidase 12 [Homo sapiens]
Gene ID:43849

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