Select Entries from OMIM -- Online Mendelian Inheritance in
Man
289 entries found, searching for "thyroid"
*190160
THYROID HORMONE RECEPTOR, BETA; THRB
*274500
THYROID HORMONOGENESIS, GENETIC DEFECT IN, IIA
#188550
THYROID CARCINOMA, PAPILLARY
*190120
THYROID HORMONE RECEPTOR, ALPHA-1; THRA
#188570
THYROID HORMONE RESISTANCE
#171400
MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2
#274300
THYROID HORMONE UNRESPONSIVENESS
*274600
PENDRED SYNDROME; PDS
*600635
THYROID TRANSCRIPTION FACTOR 1; TITF1
*602715
THYROID AND EYE MUSCLE AUTOANTIGEN, 64-KD
*274700
THYROID HORMONOGENESIS, GENETIC DEFECT IN, III
188560 THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT
*152690
THYROID AUTOANTIGEN, 70-KD; G22P1
*603372
THYROID-STIMULATING HORMONE RECEPTOR; TSHR
#145650
HYPERTHYROIDISM, FAMILIAL, DUE TO INAPPROPRIATE THYROTROPIN
SECRETION
*603386
THYROID CARCINOMA, NONMEDULLARY, WITH CELL OXYPHILIA
#155240
MEDULLARY THYROID CARCINOMA, FAMILIAL; MTC1
*188540
THYROID-STIMULATING HORMONE, BETA CHAIN; TSHB
*602617
FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 15; FKHL15
225250 ECTOPIC THYROID WITH HYPOTHYROIDISM
#275200
THYROTROPIN, UNRESPONSIVENESS TO
140300 HASHIMOTO STRUMA
*601681
PROTEASOME 26S SUBUNIT, ATPase, 5; PSMC5
#274400
THYROID HORMONOGENESIS, GENETIC DEFECT IN, I
603744 PAPILLARY THYROID MICROCARCINOMA
274900 THYROID HORMONOGENESIS, GENETIC DEFECT IN, V
*604495
NUCLEAR FACTOR OF KAPPA LIGHT CHAIN GENE ENHANCER IN B CELLS
INHIBITOR, BETA; NFKBIB
*160994
N-ACETYLGLUCOSAMINE RECEPTOR, THYROID
*176790
PROCOLLAGEN-PROLINE,2-OXOGLUTARATE-4-DIOXYGENASE, BETA SUBUNIT;
P4HB
*107950
ARRHENOBLASTOMA--THYROID ADENOMA
*601985
H4 GENE
*602848
SKELETAL MUSCLE ABUNDANT PROTEIN
*604311
PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-BINDING PROTEIN;
PPARBP
*604507
THYROID HORMONE RECEPTOR INTERACTOR 13; TRIP13
*604500
THYROID HORMONE RECEPTOR INTERACTOR 3; TRIP3
*604506
THYROID HORMONE RECEPTOR INTERACTOR 12; TRIP12
*604504
THYROID HORMONE RECEPTOR INTERACTOR 10; TRIP10
*602933
THYROID HORMONE RECEPTOR INTERACTOR 6; TRIP6
*604508
THYROID HORMONE RECEPTOR INTERACTOR 15
*604501
THYROID HORMONE RECEPTOR INTERACTOR 4; TRIP4
*604502
THYROID HORMONE RECEPTOR INTERACTOR 7; TRIP7
*604505
THYROID HORMONE RECEPTOR INTERACTOR 11; TRIP11
*604503
THYROID HORMONE RECEPTOR INTERACTOR 8; TRIP8
*300182
COFACTOR REQUIRED FOR SP1 TRANSCRIPTIONAL ACTIVATION, SUBUNIT 2,
150-KD; CRSP2
*600848
NUCLEAR RECEPTOR COREPRESSOR 2; NCOR2
188470 THYROID CARCINOMA, FOLLICULAR; FTC
*603281
2-PRIME,5-PRIME-@OLIGOADENYLATE SYNTHETASE-LIKE; OASL
*601926
THYROID HORMONE-RESPONSIVE SPOT14, RAT, HOMOLOG OF; THRSP
*188555
THYROID HORMONE-BINDING PROTEIN, CYTOSOLIC; THBP1
*602408
NUCLEAR RECEPTOR SUBFAMILY 1, GROUP D, MEMBER 1; NR1D1
*603259
MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 8; MAP3K8
*603809
THYROID HORMONE RECEPTOR-ASSOCIATED PROTEIN, 150-KD SUBUNIT
*603808
THYROID HORMONE RECEPTOR-ASSOCIATED PROTEIN, 240-KD SUBUNIT
*603810
COFACTOR REQUIRED FOR SP1 TRANSCRIPTIONAL ACTIVATION, SUBUNIT 6,
77-KD; CRSP6
304200 CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL
RETARDATION
#188530
THYROTROPIN, ALPHA CHAIN
*300188
TRINUCLEOTIDE REPEAT-CONTAINING GENE 11; TNRC11
#275100
THYROTROPIN DEFICIENCY, ISOLATED
*604062
THYROID HORMONE RECEPTOR-ASSOCIATED PROTEIN, 95-KD SUBUNIT
*274800
THYROID HORMONOGENESIS, GENETIC DEFECT IN, IV
*164761
RET PROTOONCOGENE; RET
#162300
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB; MEN2B
*167415
PAIRED BOX GENE 8; PAX8
#275000
GRAVES DISEASE
*601843
SOLUTE CARRIER FAMILY 5, MEMBER 5; SLC5A5
#218700
HYPOTHYROIDISM, ATHYREOTIC
*175100
ADENOMATOUS POLYPOSIS OF THE COLON; APC
*188450
THYROGLOBULIN; TG
*173110
POU DOMAIN, CLASS 1, TRANSCRIPTION FACTOR 1; POU1F1
*138800
GOITER, MULTINODULAR 1; MNG1
*191170
TUMOR PROTEIN p53; TP53
#158350
COWDEN DISEASE; CD
*160980
CARNEY COMPLEX; CNC
*176975
PROTEIN KINASE C, EPSILON; PRKCE
*601728
PHOSPHATASE AND TENSIN HOMOLOG; PTEN
*601984
NUCLEAR RECEPTOR COACTIVATOR 4; NCOA4
*176300
TRANSTHYRETIN; TTR
*103600
ALBUMIN; ALB
*601413
DEIODINASE, IODOTHYRONINE, TYPE II; DIO2
190445 TRIIODOTHYRONINE RECEPTOR AUXILIARY PROTEIN; TRAP
#180849
RUBINSTEIN SYNDROME
#241850
HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE
*602691
NUCLEAR RECEPTOR COACTIVATOR 1; NCOA1
*123890
CYTOTOXIC T LYMPHOCYTE-ASSOCIATED 4; CTLA4
*601038
DEIODINASE, IODOTHYRONINE, TYPE III; DIO3
#277700
WERNER SYNDROME; WRN
*114130
CALCITONIN/CALCITONIN-RELATED POLYPEPTIDE, ALPHA; CALCA
188580 THYROTOXIC PERIODIC PARALYSIS
#164970
ONCOGENE TRK
*604611
RECQ PROTEIN-LIKE 3; RECQL3
*147892
DEIODINASE, IODOTHYRONINE, TYPE I; DIO1
*602350
NEUROGRANIN; NRGN
*602209
RAS-RESPONSIVE ELEMENT BINDING PROTEIN 1; RREB1
*180240
RETINOIC ACID RECEPTOR, ALPHA; RARA
*180246
RETINOID X RECEPTOR, BETA; RXRB
*162030
NERVE GROWTH FACTOR, BETA SUBUNIT; NGFB
*252500
MUCOLIPIDOSIS II
*261680
PHOSPHOENOLPYRUVATE CARBOXYKINASE 1, SOLUBLE; PCK1
*240300
AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I
#118450
ALAGILLE SYNDROME; AGS
*600849
NUCLEAR RECEPTOR COREPRESSOR 1; NCOR1
*191315
NEUROTROPHIC TYROSINE KINASE, RECEPTOR, TYPE 1; NTRK1
*603388
GRAVES DISEASE, SUSCEPTIBILITY TO, 2
*139320
GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-STIMULATING ACTIVITY
POLYPEPTIDE 1; GNAS1
*603381
FILAMIN B, BETA; FLNB
*601538
PROPHET OF PIT1, PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR;
PROP1
*180220
RETINOIC ACID RECEPTOR, BETA; RARB
#142623
HIRSCHSPRUNG DISEASE
188455 THYROGLOSSAL DUCT CYST, FAMILIAL
*601828
NUCLEAR RECEPTOR SUBFAMILY 4, GROUP A, MEMBER 2; NR4A2
300800 ALBRIGHT HEREDITARY OSTEODYSTROPHY; AHO
269200 SCHMIDT SYNDROME
*106100
ANGIONEUROTIC EDEMA, HEREDITARY; HANE
225040 ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM
AND AGENESIS OF THE CORPUS CALLOSUM
*107741
APOLIPOPROTEIN E; APOE
*139139
NUCLEAR RECEPTOR SUBFAMILY 4, GROUP A, MEMBER 1; NR4A1
*154250
MALIC ENZYME 1; ME1
*603390
PHOSPHODIESTERASE 8B; PDE8B
*135150
FIBROFOLLICULOMAS WITH TRICHODISCOMAS AND ACROCHORDONS
*191030
TROPOMYOSIN 3; TPM3
*601993
NUCLEAR RECEPTOR COACTIVATOR 2; NCOA2
#603373
HYPERTHYROIDISM, FAMILIAL GESTATIONAL
*601972
RAR-RELATED ORPHAN RECEPTOR B; RORB
*204200
CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3
*139080
SOLUTE CARRIER FAMILY 25, MEMBER 16; SLC25A16
*160710
MYOSIN, HEAVY CHAIN 6, CARDIAC MUSCLE, ALPHA; MYH6
*601769
VITAMIN D RECEPTOR; VDR
#103580
ALBRIGHT HEREDITARY OSTEODYSTROPHY; AHO
*600542
NUCLEAR RECEPTOR SUBFAMILY 4, GROUP A, MEMBER 3; NR4A3
*600380
NUCLEAR RECEPTOR SUBFAMILY 1, GROUP H, MEMBER 2; NR1H2
*600073
LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 2; LRP2
*118910
CHROMOGRANIN A; CHGA
#171300
PHEOCHROMOCYTOMA
*602498
TRK-FUSED GENE; TFG
*114212
CALCYPHOSINE; CAPS
254200 MYASTHENIA GRAVIS; MG
*132890
NUCLEAR RECEPTOR SUBFAMILY 2, GROUP F, MEMBER 1; NR2F1
*182280
SMALL CELL CANCER OF THE LUNG
#115200
CARDIOMYOPATHY, DILATED, 1A; CMD1A
*122560
CORTICOTROPIN-RELEASING HORMONE; CRH
*145680
HYPERTHYROXINEMIA, FAMILIAL
*243800
JOHANSON-BLIZZARD SYNDROME; JBS
238800 HYPERMETABOLISM DUE TO DEFECT IN MITOCHONDRIA
*171200
PHENYLTHIOCARBAMIDE TASTING
*107773
NUCLEAR RECEPTOR SUBFAMILY 2, GROUP F, MEMBER 2; NR2F2
#174800
MCCUNE-ALBRIGHT SYNDROME; MAS
*186852
PROTEASOME 26S SUBUNIT, ATPase, 3; PSMC3
255900 MYXEDEMA
*256700
NEUROBLASTOMA
*180245
RETINOID X RECEPTOR, ALPHA; RXRA
#152700
LUPUS ERYTHEMATOSUS, SYSTEMIC; SLE
*160760
MYOSIN, HEAVY CHAIN 7, CARDIAC MUSCLE, BETA; MYH7
*160100
MYOKYMIA
*102700
ADENOSINE DEAMINASE; ADA
*114160
CALCITONIN-RELATED POLYPEPTIDE, BETA; CALCB
*180190
RETINOIC ACID RECEPTOR, GAMMA; RARG
273400 TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED
EARS, AND OTHER ABNORMALITIES
274240 THYROCEREBRORETINAL SYNDROME
219080 CUSHING DISEASE, ADRENAL
*100678
ACETYL-CoA ACETYLTRANSFERASE 2; ACAT2
602152 RHYNS SYNDROME
*604110
G PROTEIN-COUPLED RECEPTOR 56; GPR56
*604630
NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 2; NR0B2
*600239
G PROTEIN-COUPLED RECEPTOR 1; GPR1
*313700
ANDROGEN RECEPTOR; AR
*604312
CYSTATIN C; CST3
*604118
RAS PROTEIN ACTIVATOR-LIKE 1; RASAL1
304930 DIARRHEA, POLYENDOCRINOPATHY, FATAL INFECTION SYNDROME,
X-LINKED
601812 PREMATURE AGING SYNDROME, PENTTINEN TYPE
#277440
VITAMIN D-RESISTANT RICKETS WITH END-ORGAN UNRESPONSIVENESS TO
1,25-DIHYDROXYCHOLECALCIFEROL
*603046
TRANSLOCATION IN RENAL CARCINOMA ON CHROMOSOME 8
*603415
SODIUM CHANNEL, VOLTAGE-GATED, TYPE IX, ALPHA SUBUNIT; SCN9A
*602302
HAIRLESS, MOUSE, HOMOLOG OF; HR
*600825
RAR-RELATED ORPHAN RECEPTOR A; RORA
*601110
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id
*238310
HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE II
*300200
ADRENAL HYPOPLASIA, CONGENITAL; AHC
235255 MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH
LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY
301090 AMELIA, X-LINKED
229070 FOLLICLE-STIMULATING HORMONE, ISOLATED DEFICIENCY OF
*275120
THYROTROPIN-RELEASING HORMONE DEFICIENCY
241540 HYPOPITUITARISM, CONGENITAL, WITH CENTRAL DIABETES
INSIPIDUS
308050 ICHTHYOSIFORM ERYTHRODERMA, UNILATERAL, WITH IPSILATERAL
MALFORMATIONS, ESPECIALLY ABSENCE DEFORMITY OF LIMBS
*314200
THYROXINE-BINDING GLOBULIN OF SERUM; TBG
*223900
DYSAUTONOMIA, FAMILIAL; DYS
*239100
HYPEROSTOSIS CORTICALIS GENERALISATA
600146 SPASTIC PARAPLEGIA 5B, AUTOSOMAL RECESSIVE; SPG5B
*306000
GLYCOGEN STORAGE DISEASE VIII
#245150
KEUTEL SYNDROME
*307700
HYPOPARATHYROIDISM, X-LINKED; HYPX
#220700
DEAFNESS, AUTOSOMAL RECESSIVE
*219800
CYSTINOSIS, NEPHROPATHIC; CTNS
*251300
MICROCEPHALY, HIATUS HERNIA, AND NEPHROTIC SYNDROME
#253300
SPINAL MUSCULAR ATROPHY I; SMA1
*600281
HEPATOCYTE NUCLEAR FACTOR 4-ALPHA; HNF4A
#215100
RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1
#194050
WILLIAMS-BEUREN SYNDROME; WBS
*192321
VASOACTIVE INTESTINAL PEPTIDE RECEPTOR 1; VIPR1
#557000
PEARSON MARROW-PANCREAS SYNDROME
*601153
FRAGILE HISTIDINE TRIAD GENE; FHIT
*601185
STANNIOCALCIN 1; STC1
601200 PLEUROPULMONARY BLASTOMA
600084 MACROCYTOSIS, FAMILIAL
*601484
SELENOPROTEIN P, PLASMA, 1; SEPP1
*601516
ZINC FINGER PROTEIN 162; ZNF162
*601529
NUCLEAR RECEPTOR SUBFAMILY 2, GROUP C, MEMBER 1; NR2C1
*188545
THYROTROPIN-RELEASING HORMONE RECEPTOR; TRHR
*600185
BREAST CANCER 2, EARLY-ONSET; BRCA2
*186940
T-CELL ANTIGEN T4/LEU3; CD4
*185490
SUPEROXIDE DISMUTASE, EXTRACELLULAR; SOD3
*182133
5-@HYDROXYTRYPTAMINE RECEPTOR 1D; HTR1D
*262600
PITUITARY DWARFISM III
*180440
RIBONUCLEASE A FAMILY, 1; RNASE1
#262500
PITUITARY DWARFISM II
*216550
COHEN SYNDROME; COH1
*176710
PROCOLLAGEN-PROLINE,2-OXOGLUTARATE-4-DIOXYGENASE, ALPHA SUBUNIT,
ISOFORM 1; P4HA1
*601973
RETINOIC ACID RECEPTOR RESPONDER 2; RARRES2
#176410
PRECOCIOUS PUBERTY, MALE-LIMITED
*176400
PRECOCIOUS PUBERTY
#175200
PEUTZ-JEGHERS SYNDROME; PJS
*601998
ESTROGEN-RELATED RECEPTOR, ALPHA; ESRRA
*602059
IMMUNOGLOBULIN SUPERFAMILY CONTAINING LEUCINE-RICH REPEAT;
ISLR
#600791
DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 4; DFNB4
171350 PHEOCHROMOCYTOMA, FAMILIAL EXTRAADRENAL
*264090
PROGEROID SYNDROME, NEONATAL
*188595
THYROTROPH EMBRYONIC FACTOR; TEF
*171150
SULFOTRANSFERASE FAMILY 1A, PHENOL-PREFERRING, MEMBER 1;
SULT1A1
*602385
SULFOTRANSFERASE FAMILY 1C, MEMBER 1; SULT1C1
161550 NASOPHARYNGEAL CANCER
*602458
SORTILIN; SORT1
*160900
DYSTROPHIA MYOTONICA
*602575
LIM HOMEO BOX TRANSCRIPTION FACTOR 1, BETA; LMX1B
*159555
MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA; MLL
*602663
PROLACTIN-RELEASING HORMONE
*158070
ANTIGEN DEFINED BY MONOCLONAL ANTIBODY 4F2; MDU1
#153480
MACROCEPHALY, MULTIPLE LIPOMAS, AND HEMANGIOMATA
*602716
NEPHRIN
*602779
COAGULATION FACTOR II RECEPTOR-LIKE 3; F2RL3
*152790
LUTEINIZING HORMONE/CHORIOGONADOTROPIN RECEPTOR; LHCGR
*602885
G PROTEIN-COUPLED RECEPTOR 38; GPR38
#151623
LI-FRAUMENI SYNDROME; LFS
*602943
RAR-RELATED ORPHAN RECEPTOR C; RORC
*602969
ESTROGEN-RELATED RECEPTOR, GAMMA; ESRRG
*602994
LEUKOREGULIN
*601615
ATP-BINDING CASSETTE, SUBFAMILY A, MEMBER 3; ABCA3
*147940
ISLET AMYLOID POLYPEPTIDE; IAPP
*147625
ISLET CELL AUTOANTIGEN 1; ICA1
#145980
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1
*142385
HEPATIC LEUKEMIA FACTOR; HLF
*139250
GROWTH HORMONE 1; GH1
*139150
RAS p21 PROTEIN ACTIVATOR 1; RASA1
138790 GOITER, MULTINODULAR, CYSTIC RENAL DISEASE AND DIGITAL
ANOMALIES
*136435
FOLLICLE-STIMULATING HORMONE RECEPTOR; FSHR
*180247
RETINOID X RECEPTOR, GAMMA; RXRG
603736 YOUNG-SIMPSON SYNDROME
*603742
SLIT, DROSOPHILA, HOMOLOG OF, 1; SLIT1
*133430
ESTROGEN RECEPTOR 1; ESR1
*603745
SLIT, DROSOPHILA, HOMOLOG OF, 3; SLIT3
*603746
SLIT, DROSOPHILA, HOMOLOG OF, 2; SLIT2
*132880
NUCLEAR RECEPTOR SUBFAMILY 2, GROUP F, MEMBER 6; NR2F6
*131100
MULTIPLE ENDOCRINE NEOPLASIA, TYPE I; MEN1
#130650
BECKWITH-WIEDEMANN SYNDROME; BWS
*603881
NUCLEAR RECEPTOR SUBFAMILY 1, GROUP I, MEMBER 3; NR1I3
*126350
DEOXYRIBONUCLEASE II, LYSOSOMAL; DNASE2
*604090
DISCS LARGE, DROSOPHILA, HOMOLOG OF, 5; DLG5
*264300
PSEUDOHERMAPHRODITISM, MALE, WITH GYNECOMASTIA
176920 PROTEUS SYNDROME
#604129
EPIDERMOLYSIS BULLOSA PRURIGINOSA
#125853
DIABETES MELLITUS, TYPE II
#265800
PYCNODYSOSTOSIS
*604418
GAP JUNCTION PROTEIN, BETA-6; GJB6
*604429
PROLINE-RICH GAMMA-CARBOXYGLUTAMIC ACID PROTEIN 2; PRRG2
*604476
GLIOBLASTOMA OVEREXPRESSED; GOV
*123830
CYCLIC NUCLEOTIDE PHOSPHODIESTERASE; CNP
*123829
CYCLIN-DEPENDENT KINASE 4; CDK4
*117700
CERULOPLASMIN; CP
*115437
MATRILIN 1; MATN1
114190 CALCITONIN GENE-RELATED PEPTIDE RECEPTOR; CGRPR
#109100
AUTOIMMUNE DISEASES
*105250
AMYLOIDOSIS, PRIMARY CUTANEOUS
#104300
ALZHEIMER DISEASE; AD
*104220
ALPHA-1B-ADRENERGIC RECEPTOR; ADRA1B
*102775
ADENOSINE A1 RECEPTOR; ADORA1
*604517
PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA, COACTIVATOR 1;
PPARGC1
*100790
ACHAETE-SCUTE COMPLEX, DROSOPHILA, HOMOLOG-LIKE 1; ASCL1
*602221
ZINC FINGER PROTEIN 198; ZNF198
*604644
CARBONIC ANHYDRASE XI; CA11
*604645
PHOSPHODIESTERASE 7B, cAMP-SPECIFIC, HIGH-AFFINITY; PDE7B
*604662
DRE-ANTAGONIST MODULATOR