ABNORMALITY OF PRENATAL DEVELOPMENT OR BIRTH, HP:0001197

Associated diseases: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13, {PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3}, GLYCOGEN STORAGE DISEASE IV, CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1, THANATOPHORIC DYSPLASIA, TYPE II, ICHTHYOSIS, AUTOSOMAL RECESSIVE 4B (HARLEQUIN), GAUCHER DISEASE, PERINATAL LETHAL, ?MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3, BARTTER SYNDROME, TYPE 2, NEMALINE MYOPATHY 9, THANATOPHORIC DYSPLASIA, TYPE I, MYASTHENIC SYNDROME, CONGENITAL, 10, ATELOSTEOGENESIS, TYPE I, DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL, MYOTUBULAR MYOPATHY, X-LINKED, CHONDRODYSPLASIA, BLOMSTRAND TYPE, EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC STENOSIS, EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA, MYOTONIC DYSTROPHY 1, {PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1}, CEREBROCOSTOMANDIBULAR SYNDROME, HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH EXACERBATION IN PREGNANCY, MYOPATHY, ACTIN, CONGENITAL, WITH CORES, NEMALINE MYOPATHY 3, AUTOSOMAL DOMINANT OR RECESSIVE, MYOPATHY, ACTIN, CONGENITAL, WITH EXCESS OF THIN MYOFILAMENTS, CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2, TRANSALDOLASE DEFICIENCY, COLE-CARPENTER SYNDROME 2, CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB, COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3, CARDIOFACIOCUTANEOUS SYNDROME, PREGNANCY LOSS, RECURRENT, 4, SPERMATOGENIC FAILURE 4, DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA, METATROPIC DYSPLASIA, NEMALINE MYOPATHY 2, AUTOSOMAL RECESSIVE, HYPOPHOSPHATASIA, INFANTILE, NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA, NEMALINE MYOPATHY 10, WIEACKER-WOLFF SYNDROME, GALLOWAY-MOWAT SYNDROME, EHLERS-DANLOS SYNDROME, CLASSIC, EHLERS-DANLOS SYNDROME, CLASSIC TYPE, NEU-LAXOVA SYNDROME 2, PETERS-PLUS SYNDROME, LYMPHEDEMA, HEREDITARY, IA, MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL, RUBINSTEIN-TAYBI SYNDROME, PYRIDOXAMINE 5'-PHOSPHATE OXIDASE DEFICIENCY, ?MYOPATHY, CONGENITAL, COMPTON-NORTH, RENAL TUBULAR DYSGENESIS, MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7, MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14, SMITH-LEMLI-OPITZ SYNDROME, SPINAL MUSCULAR ATROPHY, X-LINKED 2, INFANTILE, MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE, DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IV, VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE, OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS, BOHRING-OPITZ SYNDROME, MENTAL RETARDATION, AUTOSOMAL DOMINANT 17, DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, SYNDROMIC, SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2, CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK, NIEMANN-PICK DISEASE TYPE C1, MECKEL SYNDROME 11, MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1, CONGENITAL MYOPATHY WITH FIBER TYPE DISPROPORTION, COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5, GREENBERG SKELETAL DYSPLASIA, KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA, FEINGOLD SYNDROME, MENTAL RETARDATION, AUTOSOMAL DOMINANT 34, ACAMPOMELIC CAMPOMELIC DYSPLASIA, CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL, CAMPOMELIC DYSPLASIA, PYRUVATE KINASE DEFICIENCY, POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY, NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VI, DIAPHANOSPONDYLODYSOSTOSIS, ?LETHAL CONGENITAL CONTRACTURE SYNDROME 6, ACHONDROGENESIS, TYPE II OR HYPOCHONDROGENESIS, VESICOURETERAL REFLUX 3, YUNIS-VARON SYNDROME, NIEMANN-PICK DISEASE, TYPE C2, WRINKLY SKIN SYNDROME, CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 3, PANCREATIC AGENESIS AND CONGENITAL HEART DEFECTS, HYDROLETHALUS SYNDROME, MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14, EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA, EHLERS-DANLOS SYNDROME, TYPE VIIB, EHLERS-DANLOS SYNDROME, TYPE VIIA, SIALIDOSIS, TYPE I, SIALIDOSIS, TYPE II, PONTOCEREBELLAR HYPOPLASIA TYPE 4, LETHAL CONGENITAL CONTRACTURE SYNDROME 1, PRADER-WILLI SYNDROME, ARTHROGRYPOSIS, DISTAL, TYPE 2A, ?TETRA-AMELIA SYNDROME, BETHLEM MYOPATHY 1, PHENYLKETONURIA, [HYPERPHENYLALANINEMIA, NON-PKU MILD], OPSISMODYSPLASIA, KEUTEL SYNDROME, PERIODIC FEVER, MENSTRUAL CYCLE DEPENDENT, VAN DEN ENDE-GUPTA SYNDROME, EPILEPSY, PYRIDOXINE-DEPENDENT, MOLYBDENUM COFACTOR DEFICIENCY C, ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS, PRETERM PREMATURE RUPTURE OF MEMBRANES, BAMFORTH-LAZARUS SYNDROME, X-INACTIVATION, FAMILIAL SKEWED, MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1, LETHAL CONGENITAL CONTRACTURE SYNDROME 9, SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY, NOONAN SYNDROME 8, ROIFMAN SYNDROME, MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA, ROBERTS SYNDROME, BARTTER SYNDROME, TYPE 1, MEIER-GORLIN SYNDROME 1, HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME, ?EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21, ?PRUNE BELLY SYNDROME, OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE 1, MUSCULAR DYSTROPHY, CONGENITAL, TRICHOHEPATOENTERIC SYNDROME 1, TRIFUNCTIONAL PROTEIN DEFICIENCY, ACHONDROGENESIS IB, LETHAL CONGENITAL CONTRACTURE SYNDROME 7, OSTEOGENESIS IMPERFECTA, TYPE II, MECKEL SYNDROME 1, KINDLER SYNDROME, GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME, ?MECKEL SYNDROME 12, VISCERAL MYOPATHY, NEMALINE MYOPATHY 8, AUTOSOMAL RECESSIVE, LETHAL CONGENITAL CONTRACTURAL SYNDROME 2, LEUKEMIA, MEGAKARYOBLASTIC, WITH OR WITHOUT DOWN SYNDROME, SOMATIC, MUCOPOLYSACCHARIDOSIS VII, EHLERS-DANLOS SYNDROME, TYPE VIIC, ARTHROGRYPOSIS, LETHAL, WITH ANTERIOR HORN CELL DISEASE, NEPHRONOPHTHISIS 2, INFANTILE, SCHNECKENBECKEN DYSPLASIA, GENITOPATELLAR SYNDROME, ?MYASTHENIC SYNDROME, CONGENITAL, 18, NON-IMMUNE HYDROPS FETALIS, PERLMAN SYNDROME, OSTEOGENESIS IMPERFECTA, TYPE VII, MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET, MILD VARIANT, MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET, THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE, {THROMBOPHILIA, SUSCEPTIBILITY TO, DUE TO FACTOR V LEIDEN}, BARTTER SYNDROME, TYPE 4B, DIGENIC, ACHONDROGENESIS, TYPE IA, ADAMS-OLIVER SYNDROME 2, HYPERTHYROIDISM, NONAUTOIMMUNE, VOHWINKEL SYNDROME, NEU-LAXOVA SYNDROME 1, ENCEPHALOPAHTY, LETHAL, DUE TO DEFECTIVE MITOCHONDRIAL PEROXISOMAL FISSION, EHLERS-DANLOS SYNDROME, TYPE IV, FIBROCHONDROGENESIS 1, D-BIFUNCTIONAL PROTEIN DEFICIENCY, SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY, MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY, PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER), CEREBROOCULOFACIOSKELETAL SYNDROME 3, SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY, FETAL AKINESIA DEFORMATION SEQUENCE, ?FETAL AKINESIA DEFORMATION SEQUENCE, MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS, RITSCHER-SCHINZEL SYNDROME 1, AUTOSOMAL RECESSIVE CUTIS LAXA TYPE IA, COSTELLO SYNDROME, CONGENITAL MYOPATHY WITH EXCESS OF MUSCLE SPINDLES, SIALIC ACID STORAGE DISORDER, INFANTILE, CPT DEFICIENCY, HEPATIC, TYPE IA, {PREECLAMPSIA, SUSCEPTIBILITY TO}, {HYPERTENSION, PREGNANCY-INDUCED}, ?RENAL-HEPATIC-PANCREATIC DYSPLASIA 2, ESCOBAR SYNDROME, RESTRICTIVE DERMOPATHY, LETHAL, CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA, ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS, SENSORINEURAL DEAFNESS WITH MILD RENAL DYSFUNCTION, BARTTER SYNDROME, TYPE 4A, ACROFACIAL DYSOSTOSIS 1, NAGER TYPE, SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE, MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2, LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3, INSULIN RESISTANCE, SEVERE, DIGENIC, HYPERTHYROIDISM, FAMILIAL GESTATIONAL, IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME, RENAL ADYSPLASIA, SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY, EHLERS-DANLOS SYNDROME, TYPE VI, PREECLAMPSIA/ECLAMPSIA 5, LETHAL CONGENITAL CONTRACTURE SYNDROME 5, {PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2}, CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2, RENAL-HEPATIC-PANCREATIC DYSPLASIA 1, MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY, HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS, SPINAL MUSCULAR ATROPHY-1, DENTATORUBRO-PALLIDOLUYSIAN ATROPHY, POLYCYSTIC KIDNEY AND HEPATIC DISEASE, CHONDRODYSPLASIA PUNCTATA, X-LINKED DOMINANT, CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME, CODAS SYNDROME, CPT II DEFICIENCY, LETHAL NEONATAL, LEUKODYSTROPHY, HYPOMYELINATING, 3, DIAMOND-BLACKFAN ANEMIA 1, PREECLAMPSIA/ECLAMPSIA 4, SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY, AU-KLINE SYNDROME, PROLIFERATIVE VASCULOPATHY AND HYDRAENCEPHALY-HYDROCEPHALY SYNDROME

Associated genes: LMNA, DNM2, F2, WDR73, CNTNAP1, COL1A1, CPT2, CHRNG, NECAP1, F5, LBR, COL1A2, EBP, UBN1, B3GLCT, AGT, PMM2, PPARG, AGTR1, ZBTB42, PPP1R3A, NPC1, UBA1, KIF14, TMEM231, ADGRG6, SLC17A5, COL6A1, CBL, ALG1, IBA57, CLASP1, TRIP11, MMP1, NEK8, MMP8, PKHD1, PNPO, EFEMP2, BMPER, POR, MBTPS2, ATN1, MKS1, CREBBP, ESCO2, COL2A1, ATP6V0A2, SF3B4, MUSK, FIG4, ACTA1, PLOD1, ACE, COL6A2, DOK7, TRPV4, FBLN5, ERBB3, MEGF10, ABCA12, CLCNKA, MYH7, GBE1, MRPS22, CDAN1, ALDH7A1, MYCN, SPINT2, TTC37, BUB1B, WDR34, RYR1, EPHX1, STOX1, NOS3, KCNJ11, COL3A1, ZC4H2, HADHA, KIF5C, DOCK6, LONP1, CHRND, KCNJ1, THSD1, MYOM1, PTH1R, MTM1, TALDO1, KAT6B, ZMPSTE24, SOX9, CRTAP, COL5A1, ERCC5, ADAMTS2, PIGC, GUSB, TSHR, TNNT2, NR3C2, CLCNKB, ATP8B1, GPHN, ANXA5, BRAF, KLHL40, SLC26A3, DNM1L, SNAP25, POMP, SLC12A1, GATA1, ISPD, RNU4ATAC, DIS3L2, LMOD3, ALPL, ITGA8, PEX1, KIAA0586, SNRPB, PLEC, FLT4, DNAH14, TMCO1, SNRPN, TSFM, CHRM3, GMPPB, REN, CNTN1, GALNT14, TTC7A, TMEM70, RAPSN, CHRNA1, HRAS, SOX17, XIST, CORIN, HADHB, NPHP3, PSAT1, WDR35, WDR62, HTR1A, SOX18, ABCB4, NDN, PHGDH, COX15, HNRNPK, BSND, RPS19, ORC1, SEC24D, FGFR3, SMN1, FZD6, NPC2, AMER1, INPPL1, ITGA6, COL6A3, PAH, GLE1, HSD17B4, SLC26A2, CHRNE, PIGN, INVS, AIMP1, IGHMBP2, GJB2, SEPN1, KLHL41, ASXL1, DHCR7, MYH3, ITGB4, WNT3, HYLS1, GATA6, KLF1, COL11A1, DMPK, UPK3A, FERMT1, NEK1, PKLR, KIAA0196, SERPINH1, SCARF2, FLVCR2, ZNF592, PACS1, FOXE1, WDR60, COL5A2, GBA, SYCP3, CPT1A, NEU1, OFD1, STRADA, RET, RIT1, FOXF1, FLNB, CRB2, TSEN54, SARS2, MGP, COL4A3BP, MYH11, ALB, NEB, SLC35D1, ACTG2, TPM3, MAP2K2