gi|19112691|ref|NP_595899.1| - OMIM - NCBI

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The following terms were not found in OMIM: 19112691, NP_595899.1.

Select item 6041711.

*604171 - ALY/REF EXPORT FACTOR; ALYREF

OMIM:: 604171

Gene summaries Genetic tests Medical literature

Select item 6115202.

*611520 - POLYMERASE DELTA-INTERACTING PROTEIN 3; POLDIP3

Cytogenetic locations: 168890

OMIM:: 611520

Gene summaries Genetic tests Medical literature

Select item 6196283.

*619628 - AFTIPHILIN; AFTPH

Cytogenetic locations: ##gI##

OMIM:: 619628

Gene summaries Genetic tests Medical literature

Select item 1393104.

*139310 - GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-INHIBITING ACTIVITY POLYPEPTIDE 1; GNAI1

Cytogenetic locations: Clip2

OMIM:: 139310

Gene summaries Genetic tests Medical literature

Select item 2075005.

207500 - ANUS, IMPERFORATE

OMIM:: 207500

Gene summaries Genetic tests Medical literature

Select item 2357506.

235750 - HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIG TOES, AND VENTRICULAR SEPTAL DEFECT

OMIM:: 235750

Gene summaries Genetic tests Medical literature

Select item 2194007.

219400 - CYANOSIS AND HEPATIC DISEASE

OMIM:: 219400

Gene summaries Genetic tests Medical literature

Select item 1643308.

164330 - ODONTOMA-DYSPHAGIA SYNDROME

OMIM:: 164330

Gene summaries Genetic tests Medical literature

Select item 2025509.

202550 - AGANGLIONOSIS, TOTAL INTESTINAL

OMIM:: 202550

Gene summaries Genetic tests Medical literature

Select item 17540010.

175400 - POLYPOSIS, INTESTINAL, SCATTERED AND DISCRETE

OMIM:: 175400

Gene summaries Genetic tests Medical literature

Select item 23574011.

235740 - HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS

OMIM:: 235740

Gene summaries Genetic tests Medical literature

Select item 20977012.

209770 - AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION

OMIM:: 209770

Gene summaries Genetic tests Medical literature

Select item 13324013.

133240 - ESOPHAGEAL RING, LOWER

OMIM:: 133240

Gene summaries Genetic tests Medical literature

Select item 23290014.

232900 - GLYCOPROTEIN STORAGE DISEASE

OMIM:: 232900

Gene summaries Genetic tests Medical literature

Select item 13704015.

137040 - GALLBLADDER, AGENESIS OF

OMIM:: 137040

Gene summaries Genetic tests Medical literature

Select item 22135016.

%221350 - DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA

OMIM:: 221350

Gene summaries Genetic tests Medical literature

Select item 14090017.

140900 - HEMANGIOMAS OF SMALL INTESTINE

OMIM:: 140900

Gene summaries Genetic tests Medical literature

Select item 31219018.

312190 - RADIAL APLASIA, X-LINKED

OMIM:: 312190

Gene summaries Genetic tests Medical literature

Select item 12044019.

120440 - COLONIC VARICES WITHOUT PORTAL HYPERTENSION

OMIM:: 120440

Gene summaries Genetic tests Medical literature

Select item 17545020.

175450 - POLYPOSIS, INTESTINAL, WITH MULTIPLE EXOSTOSES

OMIM:: 175450

Gene summaries Genetic tests Medical literature

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