Pain - OMIM - NCBI

Pain - 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 "Pain" 

112270 - BONE PAIN, PERIODIC

OMIM:

 

112270

Gene summaries Genetic tests Medical literature

Select item 1475302.

147530 - INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY

OMIM:

 

147530

Gene summaries Genetic tests Medical literature

Select item 2605703.

260570 - PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN

OMIM:

 

260570

Gene summaries Genetic tests Medical literature

Select item 2128904.

212890 - CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA

OMIM:

 

212890

Gene summaries Genetic tests Medical literature

Select item 1674005.

#167400 - PAROXYSMAL EXTREME PAIN DISORDER

Cytogenetic locations: 2q24.3

OMIM:

 

167400

Gene summaries Genetic tests Medical literature

Select item 6150406.

#615040 - EPISODIC PAIN SYNDROME, FAMILIAL, 1; FEPS1

Cytogenetic locations: 8q21.11

OMIM:

 

615040

Gene summaries Genetic tests Medical literature

Select item 6155517.

#615551 - EPISODIC PAIN SYNDROME, FAMILIAL, 2; FEPS2

Cytogenetic locations: 3p22.2

OMIM:

 

615551

Gene summaries Genetic tests Medical literature

Select item 1474308.

#147430 - MARSILI SYNDROME; MARSIS

Cytogenetic locations: 14q11.2

OMIM:

 

147430

Gene summaries Genetic tests Medical literature

Select item 2430009.

#243000 - INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID, INCLUDED; HSAN2D, INCLUDED

Cytogenetic locations: 2q24.3

OMIM:

 

243000

Gene summaries Genetic tests Medical literature

Select item 61554810.

#615548 - NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7

Cytogenetic locations: 3p22.2

OMIM:

 

615548

Gene summaries Genetic tests Medical literature

Select item 61555211.

#615552 - EPISODIC PAIN SYNDROME, FAMILIAL, 3; FEPS3

Cytogenetic locations: 3p22.2

OMIM:

 

615552

Gene summaries Genetic tests Medical literature

Select item 61745012.

#617450 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAINTHRESHOLD; IDDGIP

Cytogenetic locations: 17q23.2

OMIM:

 

617450

Gene summaries Genetic tests Medical literature

Select item 60865413.

#608654 - NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V; HSAN5

Cytogenetic locations: 1p13.2

OMIM:

 

608654

Gene summaries Genetic tests Medical literature

Select item 25680014.

#256800 - INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA

Cytogenetic locations: 1q23.1

OMIM:

 

256800

Gene summaries Genetic tests Medical literature

Select item 11687015.

116870 - CELIAC ARTERY STENOSIS FROM COMPRESSION BY MEDIAN ARCUATE LIGAMENT OF DIAPHRAGM

OMIM:

 

116870

Gene summaries Genetic tests Medical literature

Select item 16645016.

166450 - OSTEOMESOPYKNOSIS

OMIM:

 

166450

Gene summaries Genetic tests Medical literature

Select item 60822017.

%608220 - SPASTIC PARAPLEGIA 25, AUTOSOMAL RECESSIVE; SPG25

Cytogenetic locations: 6q23-q24.1

OMIM:

 

608220

Gene summaries Genetic tests Medical literature

Select item 11861018.

118610 - CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION

OMIM:

 

118610

Gene summaries Genetic tests Medical literature

Select item 16890019.

%168900 - PATELLA, CHONDROMALACIA OF

OMIM:

 

168900

Gene summaries Genetic tests Medical literature

Select item 18295020.

%182950 - SPINAL ARACHNOIDITIS

OMIM:

 

182950

Gene summaries Genetic tests Medical literature