full length OR span - OMIM

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Select item 1368901.

*136890 - FULL-LENGTH RETROVIRAL SEQUENCE 3; FRV3

OMIM:: 136890

Gene summaries Genetic tests Medical literature

Select item 1368702.

*136870 - FULL-LENGTH RETROVIRAL SEQUENCE 2; FRV2

OMIM:: 136870

Gene summaries Genetic tests Medical literature

Select item 1368403.

*136840 - FULL-LENGTH RETROVIRAL SEQUENCE 1; FRV1

OMIM:: 136840

Gene summaries Genetic tests Medical literature

Select item 6123124.

%612312 - ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 6

Cytogenetic locations: Protein

OMIM:: 612312

Gene summaries Genetic tests Medical literature

Select item 6088335.

*608833 - REGULATOR OF TELOMERE ELONGATION HELICASE 1; RTEL1

Cytogenetic locations: 29671732

OMIM:: 608833

Gene summaries Genetic tests Medical literature

Select item 2487706.

248770 - MARFANOID IMPAIRED INTELLECTUAL DEVELOPMENTAL SYNDROME, AUTOSOMAL

OMIM:: 248770

Gene summaries Genetic tests Medical literature

Select item 1175507.

#117550 - SOTOS SYNDROME; SOTOS

Cytogenetic locations: 14889595

OMIM:: 117550

Gene summaries Genetic tests Medical literature

Select item 1943208.

194320 - WORONETS TRAIT

OMIM:: 194320

Gene summaries Genetic tests Medical literature

Select item 1547009.

#154700 - MARFAN SYNDROME; MFS

Cytogenetic locations: 208500

OMIM:: 154700

Gene summaries Genetic tests Medical literature

Select item 22337010.

%223370 - DUBOWITZ SYNDROME

OMIM:: 223370

Gene summaries Genetic tests Medical literature

Select item 61406311.

#614063 - N-ACETYLASPARTATE DEFICIENCY; NACED

Cytogenetic locations: Pak2

OMIM:: 614063

Gene summaries Genetic tests Medical literature

Select item 61625512.

#616255 - SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES 1; SNSK1

Cytogenetic locations: 24001744

OMIM:: 616255

Gene summaries Genetic tests Medical literature

Select item 61380513.

#613805 - MEIER-GORLIN SYNDROME 5; MGORS5

Cytogenetic locations: 11477602

OMIM:: 613805

Gene summaries Genetic tests Medical literature

Select item 30055814.

#300558 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 30; XLID30

Cytogenetic locations: 18523455

OMIM:: 300558

Gene summaries Genetic tests Medical literature

Select item 61021715.

#610217 - NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B

KARAK SYNDROME, INCLUDED

Cytogenetic locations: 22q11.21

OMIM:: 610217

Gene summaries Genetic tests Medical literature

Select item 61860316.

#618603 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB

Cytogenetic locations: 603020

OMIM:: 618603

Gene summaries Genetic tests Medical literature

Select item 62068817.

#620688 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 74; MRD74

OMIM:: 620688

Gene summaries Genetic tests Medical literature

Select item 61958018.

#619580 - NEURODEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND ATAXIA AND WITH OR WITHOUT SEIZURES; NEDLAS

Cytogenetic locations: 34375587

OMIM:: 619580

Gene summaries Genetic tests Medical literature

Select item 23870019.

#238700 - HYPERLYSINEMIA, TYPE I

Cytogenetic locations: 14753051

OMIM:: 238700

Gene summaries Genetic tests Medical literature

Select item 25175020.

#251750 - MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA

Cytogenetic locations: 20617341

OMIM:: 251750

Gene summaries Genetic tests Medical literature

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