OMIM for BioSystems (Select 1285075) - OMIM - NCBI

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Items: 1 to 20 of 164

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Select item 6205201.

*620520 - CALMODULIN-LIKE 4; CALML4

Cytogenetic locations: 607856

OMIM:: 620520

Gene summaries Genetic tests Medical literature

Select item 6204582.

#620458 - AURICULOCONDYLAR SYNDROME 2B; ARCND2B

Cytogenetic locations: P##A##

OMIM:: 620458

Gene summaries Genetic tests Medical literature

Select item 6202463.

#620246 - CONGENITAL MYOPATHY 18; CMYP18

OMIM:: 620246

Gene summaries Genetic tests Medical literature

Select item 6201144.

#620114 - NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND WITH OR WITHOUT SEIZURES; NEDSIS

Cytogenetic locations: #(G###

OMIM:: 620114

Gene summaries Genetic tests Medical literature

Select item 6201115.

#620111 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1J; CMT1J

Cytogenetic locations: #5#@##

OMIM:: 620111

Gene summaries Genetic tests Medical literature

Select item 6200296.

#620029 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, LANGUAGE DELAY, AND SKELETAL DEFECTS WITH OR WITHOUT SEIZURES; NEDHLSS

Cytogenetic locations: 605170

OMIM:: 620029

Gene summaries Genetic tests Medical literature

Select item 6199117.

#619911 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND EARLY-ONSET DOPA-RESPONSIVE DYSTONIA-PARKINSONISM; IDLDP

Cytogenetic locations: P#?###

OMIM:: 619911

Gene summaries Genetic tests Medical literature

Select item 6196518.

#619651 - NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS AND DYSKINESIA; NEDHYD

Cytogenetic locations: 601199

OMIM:: 619651

Gene summaries Genetic tests Medical literature

Select item 6196479.

#619647 - DYSKINESIA WITH OROFACIAL INVOLVEMENT, AUTOSOMAL RECESSIVE; DSKOR

Cytogenetic locations: 601199

OMIM:: 619647

Gene summaries Genetic tests Medical literature

Select item 61932410.

#619324 - HYPERTRIGLYCERIDEMIA 2; HYTG2

Cytogenetic locations: ###a##

OMIM:: 619324

Gene summaries Genetic tests Medical literature

Select item 61915011.

#619150 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES; IDDPADS

Cytogenetic locations: 600466

OMIM:: 619150

Gene summaries Genetic tests Medical literature

Select item 61914312.

#619143 - CARDIOACROFACIAL DYSPLASIA 2; CAFD2

Cytogenetic locations: `#####

OMIM:: 619143

Gene summaries Genetic tests Medical literature

Select item 61914213.

#619142 - CARDIOACROFACIAL DYSPLASIA 1; CAFD1

Cytogenetic locations: PwU###

OMIM:: 619142

Gene summaries Genetic tests Medical literature

Select item 61896114.

#618961 - SPONDYLOMETAPHYSEAL DYSPLASIA WITH CORNEAL DYSTROPHY; SMDCD

Cytogenetic locations: B3gat3

OMIM:: 618961

Gene summaries Genetic tests Medical literature

Select item 61878215.

#618782 - LONG QT SYNDROME 16; LQT16

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC 6, INCLUDED; CPVT6, INCLUDED

Cytogenetic locations: pJVU##

OMIM:: 618782

Gene summaries Genetic tests Medical literature

Select item 61852216.

#618522 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59; MRD59

Cytogenetic locations: Apoptosis-inducing

OMIM:: 618522

Gene summaries Genetic tests Medical literature

Select item 61844717.

#618447 - LONG QT SYNDROME 8; LQT8

Cytogenetic locations: 605170

OMIM:: 618447

Gene summaries Genetic tests Medical literature

Select item 61826218.

*618262 - cAMP RESPONSE ELEMENT-BINDING PROTEIN 5; CREB5

Cytogenetic locations: #########c#

OMIM:: 618262

Gene summaries Genetic tests Medical literature

Select item 61809519.

#618095 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 63; MRT63

Cytogenetic locations: 0##5##

OMIM:: 618095

Gene summaries Genetic tests Medical literature

Select item 61808720.

#618087 - SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND

Cytogenetic locations: PY####

OMIM:: 618087

Gene summaries Genetic tests Medical literature

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