X-linked inheritance
Symptom Information:
| Symptom ID: | HPO:0001417 | ||
| Synonyms: |
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| Quality: | |||
| Cross references: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Mode of inheritance(HPO:0000005) Gonosomal inheritance(HPO:0010985) X-linked inheritance(HPO:0001417) MedDRA: |
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| Database Frequency: | 173 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 46,XY SEX REVERSAL 2 | (OMIM:300018) |
| 6-@PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE 1 | (OMIM:311790) |
| ALOPECIA, CONGENITAL | (OMIM:300042) |
| AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2 | (OMIM:301201) |
| ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE | (OMIM:206000) |
| ANOSMIA | (OMIM:301700) |
| ANUS, IMPERFORATE | (OMIM:301800) |
| ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 | (OMIM:300494) |
| ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 | (OMIM:300497) |
| AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 | (OMIM:300425) |
| AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 | (OMIM:300495) |
| AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 | (OMIM:300496) |
| Aarskog-Scott syndrome | (Orphanet:915) |
| Abruzzo-Erickson syndrome | (Orphanet:921) |
| Adrenomyodystrophy | (Orphanet:977) |
| Albinism-deafness syndrome | (Orphanet:998) |
| Bullous dystrophy, macular type | (Orphanet:1867) |
| CALBINDIN 3 | (OMIM:302020) |
| CALVARIAL HYPEROSTOSIS | (OMIM:302030) |
| CATARACT 40 | (OMIM:302200) |
| CENTRAL INCISORS, ABSENCE OF | (OMIM:302400) |
| CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 1 | (OMIM:302650) |
| CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE | (OMIM:302700) |
| CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
| CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE | (OMIM:118230) |
| CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
| CHROMOSOME Xp11.22 DUPLICATION SYNDROME | (OMIM:300705) |
| CLARK-BARAITSER SYNDROME | (OMIM:300602) |
| CONE-ROD DYSTROPHY, X-LINKED, 2 | (OMIM:300085) |
| CORNELIA DE LANGE SYNDROME 5 | (OMIM:300882) |
| Cantrell pentalogy | (Orphanet:1335) |
| Cerebellum agenesis - hydrocephaly | (Orphanet:1397) |
| Christianson syndrome | (Orphanet:85278) |
| Contractures - ectodermal dysplasia - cleft lip/palate | (Orphanet:1484) |
| DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE | (OMIM:304900) |
| ELK1, MEMBER OF ETS ONCOGENE FAMILY | (OMIM:311040) |
| EPIDERMODYSPLASIA VERRUCIFORMIS, X-LINKED | (OMIM:305350) |
| EPISODIC MUSCLE WEAKNESS, X-LINKED | (OMIM:300211) |
| Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
| Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
| FETAL AKINESIA SYNDROME, X-LINKED | (OMIM:300073) |
| FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 3 | (OMIM:305435) |
| FG SYNDROME 2 | (OMIM:300321) |
| FG SYNDROME 4 | (OMIM:300422) |
| FORKHEAD BOX O4 | (OMIM:300033) |
| Familial isolated hypoparathyroidism due to agenesis of parathyroid gland | (Orphanet:2239) |
| Female restricted epilepsy with intellectual deficit | (Orphanet:101039) |
| Fingerprint body myopathy | (Orphanet:97232) |
| GAMMA-AMINOBUTYRIC ACID RECEPTOR, ALPHA-3 | (OMIM:305660) |
| GASTRIN-RELEASING PEPTIDE RECEPTOR | (OMIM:305670) |
| GENITOURINARY TRACT ANOMALIES | (OMIM:305690) |
| HEMOPHILIA A WITH VASCULAR ABNORMALITY | (OMIM:306800) |
| HEMOPOIETIC PROLIFERATION | (OMIM:306930) |
| HETEROTAXY, VISCERAL, 1, X-LINKED | (OMIM:306955) |
| HYPOGONADISM, MALE | (OMIM:307300) |
| HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA | (OMIM:308700) |
| ICHTHYOSIS AND MALE HYPOGONADISMRUD SYNDROME, INCLUDED | (OMIM:308200) |
| IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACEGLYCOPROTEIN | (OMIM:308220) |
| IMMUNOGLOBULIN M, LEVEL OF | (OMIM:308250) |
| IMPACTED TEETH, MULTIPLE | (OMIM:308280) |
| IRIS HYPOPLASIA WITH GLAUCOMA | (OMIM:308500) |
| Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures | (Orphanet:1568) |
| Intellectual deficit, X-linked - plagiocephaly | (Orphanet:2898) |
| Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
| Intellectual deficit, X-linked, Miles-Carpenter type | (Orphanet:85283) |
| Intellectual deficit, X-linked, Raymond type | (Orphanet:163953) |
| Intellectual deficit, X-linked, Schimke type | (Orphanet:85285) |
| Intellectual deficit, X-linked, Turner type | (Orphanet:85328) |
| Isolated agammaglobulinemia | (Orphanet:229717) |
| Isolated breast aplasia | (Orphanet:180188) |
| Isolated congenital megalocornea | (Orphanet:91489) |
| Isolated growth hormone deficiency type III | (Orphanet:231692) |
| KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA | (OMIM:308750) |
| Keratosis follicularis - dwarfism - cerebral atrophy | (Orphanet:2339) |
| LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME | (OMIM:308940) |
| LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT | (OMIM:308950) |
| LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
| Lissencephaly type 1 due to doublecortin gene mutation | (Orphanet:2148) |
| MACULAR DYSTROPHY, X-LINKED | (OMIM:309100) |
| MCF.2 CELL LINE-DERIVED TRANSFORMING SEQUENCE | (OMIM:311030) |
| MENTAL RETARDATION, X-LINKED 14 | (OMIM:300062) |
| MENTAL RETARDATION, X-LINKED 19 | (OMIM:300844) |
| MENTAL RETARDATION, X-LINKED 20 | (OMIM:300047) |
| MENTAL RETARDATION, X-LINKED 41 | (OMIM:300849) |
| MENTAL RETARDATION, X-LINKED 49 | (OMIM:300114) |
| MENTAL RETARDATION, X-LINKED 50 | (OMIM:300115) |
| MENTAL RETARDATION, X-LINKED 58 | (OMIM:300210) |
| MENTAL RETARDATION, X-LINKED 63 | (OMIM:300387) |
| MENTAL RETARDATION, X-LINKED 73 | (OMIM:300355) |
| MENTAL RETARDATION, X-LINKED 88 | (OMIM:300852) |
| MENTAL RETARDATION, X-LINKED 9 | (OMIM:309549) |
| MENTAL RETARDATION, X-LINKED 90 | (OMIM:300850) |
| MENTAL RETARDATION, X-LINKED 91 | (OMIM:300577) |
| MENTAL RETARDATION, X-LINKED 92 | (OMIM:300851) |
| MENTAL RETARDATION, X-LINKED 95 | (OMIM:300716) |
| MENTAL RETARDATION, X-LINKED 97 | (OMIM:300803) |
| MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
| MICROPHTHALMIA, SYNDROMIC 13 | (OMIM:300915) |
| MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 | (OMIM:300125) |
| MODIFIER, X-LINKED, FOR NEUROFUNCTIONAL DEFECTS | (OMIM:309840) |
| MONOAMINE OXIDASE A | (OMIM:309850) |
| MONOAMINE OXIDASE B | (OMIM:309860) |
| MUSCULAR DYSTROPHY, CARDIAC TYPE | (OMIM:309930) |
| MUSCULAR DYSTROPHY, MABRY TYPE | (OMIM:310000) |
| MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL | (OMIM:310095) |
| MYOCLONIC EPILEPSY, PROGRESSIVE | (OMIM:310370) |
| MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
| Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies | (Orphanet:2234) |
| Methylmalonic acidemia with homocystinuria, type cblX | (Orphanet:369962) |
| Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
| Microphthalmia - ankyloblepharon - intellectual deficit | (Orphanet:85275) |
| Morse-Rawnsley-Sargent syndrome | (Orphanet:2570) |
| N syndrome | (Orphanet:2608) |
| NEURAL TUBE DEFECTS, X-LINKEDSPINA BIFIDA, X-LINKED, INCLUDED | (OMIM:301410) |
| NEUROPATHY, HEREDITARY SENSORY, X-LINKED | (OMIM:310470) |
| NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A | (OMIM:300071) |
| NYSTAGMUS 6, CONGENITAL, X-LINKED | (OMIM:300814) |
| OCCIPITAL HAIR, WHITE LOCK OF | (OMIM:310900) |
| OMPHALOCELE, X-LINKED | (OMIM:310980) |
| OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA | (OMIM:311000) |
| OPTIC ATROPHY--SPASTIC PARAPLEGIA SYNDROME | (OMIM:311100) |
| OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA | (OMIM:311150) |
| OUABAIN RESISTANCE | (OMIM:311350) |
| Ocular albinism with congenital sensorineural deafness | (Orphanet:352740) |
| Ocular albinism with late-onset sensorineural deafness | (Orphanet:1000) |
| PAINE SYNDROME | (OMIM:311400) |
| PANHYPOPITUITARISM, X-LINKED | (OMIM:312000) |
| PREMATURE OVARIAN FAILURE 1 | (OMIM:311360) |
| PROSTATE CANCER, HEREDITARY, X-LINKED 1 | (OMIM:300147) |
| PSEUDOHERMAPHRODITISM, INCOMPLETE MALE, TYPE I | (OMIM:312100) |
| Pierre Robin syndrome - faciodigital anomaly | (Orphanet:2888) |
| RADIAL LOOP, PLAIN, ON RIGHT INDEX FINGER | (OMIM:312200) |
| RADIATION SENSITIVITY OF NATURAL KILLER ACTIVITY | (OMIM:312210) |
| RENIN-BINDING PROTEIN | (OMIM:312420) |
| RETICULOENDOTHELIOSIS, X-LINKED | (OMIM:312500) |
| RETINITIS PIGMENTOSA 2 | (OMIM:312600) |
| RETINITIS PIGMENTOSA 24 | (OMIM:300155) |
| RETINITIS PIGMENTOSA 3 | (OMIM:300029) |
| RIBOSOMAL PROTEIN S4, X-LINKED | (OMIM:312760) |
| Radius absent - anogenital anomalies | (Orphanet:3016) |
| SOLUTE CARRIER FAMILY 10 (SODIUM/BILE ACID COTRANSPORTER FAMILY) MEMBER3 | (OMIM:312090) |
| SPINOCEREBELLAR ATAXIA, X-LINKED 2 | (OMIM:302600) |
| SPLIT-HAND/FOOT MALFORMATION 2 | (OMIM:313350) |
| SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 4 | (OMIM:300770) |
| Severe X-linked intellectual deficit, Gustavson type | (Orphanet:3078) |
| Shox-related short stature | (Orphanet:314795) |
| Skeletal dysplasia - intellectual deficit | (Orphanet:1436) |
| Spastic paraparesis - deafness | (Orphanet:2815) |
| Spondylometaphyseal dysplasia, Golden type | (Orphanet:168544) |
| TARP syndrome | (Orphanet:2886) |
| TESTICULAR GERM CELL TUMOR 1 | (OMIM:300228) |
| THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE | (OMIM:314000) |
| THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT | (OMIM:300807) |
| TOOTH SIZE | (OMIM:314240) |
| UNIQUE GREEN PHENOMENON | (OMIM:314380) |
| V-RAF MURINE SARCOMA 3611 VIRAL ONCOGENE HOMOLOG 1 | (OMIM:311010) |
| VESICOURETERAL REFLUX, X-LINKED | (OMIM:314550) |
| W syndrome | (Orphanet:2804) |
| X-linked cleft palate and ankyloglossia | (Orphanet:324601) |
| X-linked complicated corpus callosum dysgenesis | (Orphanet:1497) |
| X-linked corneal dermoid | (Orphanet:1661) |
| X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia | (Orphanet:317476) |
| X-linked lethal multiple pterygium syndrome | (Orphanet:79447) |
| X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |
| X-linked lymphoproliferative disease | (Orphanet:2442) |
| X-linked mandibulofacial dysostosis | (Orphanet:1131) |
| X-linked recessive ocular albinism | (Orphanet:54) |
| X-linked reticulate pigmentary disorder with systemic manifestations | (Orphanet:85453) |
| X-linked retinal dysplasia | (Orphanet:1852) |
| X-linked spinocerebellar ataxia type 4 | (Orphanet:85292) |
| XM SYSTEM | (OMIM:314900) |
| ZINC FINGER PROTEIN, X-LINKED | (OMIM:314980) |
| Åland Islands eye disease | (Orphanet:178333) |