Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 836 for without
  1. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart (NEDBEH) is a neurological disorder that can also affect many other body systems. ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  2. RIT1 gene 
    ... GTP-binding protein Roc1 MGC125864 MGC125865 Ras-like without CAAX 1 ras-like without CAAX protein 1 RIBB RIT ROC1 Tests of RIT1 PubMed RIC-LIKE PROTEIN WITHOUT CAAX MOTIF 1; RIT1 NCBI Gene ClinVar Berger ...
    https://medlineplus.gov/genetics/gene/rit1 - Genetics
  3. Migraine 
    ... migraine. In some cases, an aura can occur without a subsequent migraine.In the headache phase, the ... associated with the development of migraines with or without aura. These genes likely have varying degrees of ...
    https://medlineplus.gov/genetics/condition/migraine - Genetics
  4. Asphyxiating thoracic dystrophy 
    ... gov SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1 SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6 SHORT-RIB THORACIC DYSPLASIA 9 WITH ...
    https://medlineplus.gov/.../asphyxiating-thoracic-dystrophy - Genetics
  5. CUL3-related neurodevelopmental disorder 
    ... cases, no cullin-3 protein production at all. Without the normal amount of functioning cullin-3 proteins, ... in their family. NEDAUS Neurodevelopmental disorder with or without autism or seizures Genetic Testing Registry: Neurodevelopmental disorder ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  6. CASK-related intellectual disability 
    ... X-linked intellectual disability (XL-ID) with or without nystagmus. Within each of these forms, males typically ... form of the disorder.XL-ID with or without nystagmus (rapid, involuntary eye movements) is a milder ...
    https://medlineplus.gov/.../cask-related-intellectual-disability - Genetics
  7. Danon disease 
    ... first experience health problems in childhood or adolescence; without treatment, these individuals typically live into early adulthood. ... early adulthood and typically survive into mid-adulthood without treatment.Cardiomyopathy is the most common symptom of ...
    https://medlineplus.gov/genetics/condition/danon-disease - Genetics
  8. Action myoclonus–renal failure syndrome 
    ... syndrome AMRF Epilepsy, progressive myoclonic 4, with or without renal failure EPM4 Familial myoclonus with renal failure ... Disorders (NORD) EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4 PubMed Balreira A, Gaspar P, ...
    https://medlineplus.gov/.../action-myoclonus-renal-failure-syndrome - Genetics
  9. Epilepsy-aphasia spectrum 
    ... percent of people with CECTS. In affected people without a GRIN2A gene variant, the cause of the ... Focal epilepsy with speech disorder and with or without mental retardation Landau-Kleffner syndrome National Organization for ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  10. VLDLR-associated cerebellar hypoplasia 
    ... cells from producing any functional VLDL receptor protein. Without this protein, developing nerve cells cannot reach the ... retardation Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion Cerebellar hypoplasia, VLDLR-associated CHMRQ1 DES- ...
    https://medlineplus.gov/.../vldlr-associated-cerebellar-hypoplasia - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next