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146 Possible Causes for Short Stature (79%)

Did you mean: Short Stature (79, )

  • Arthrogryposis-Renal Dysfunction-Cholestasis Syndrome

    […] of people have these symptoms Cachexia Wasting syndrome 0004326 Short stature Decreased body height Small stature [ more ] 0004322 Percent of people who have these symptoms[rarediseases.info.nih.gov] […] appearance 0000346 30%-79% of people have these symptoms EEG abnormality 0002353 Intrauterine growth retardation Prenatal growth deficiency Prenatal growth retardation [[rarediseases.info.nih.gov] Arachnodactyly Long slender fingers Spider fingers [ more ] 0001166 Joint stiffness Stiff joint Stiff joints [ more ] 0001387 Sensorineural hearing impairment 0000407 30%-79%[rarediseases.info.nih.gov]

  • Kohlschütter-Tönz Syndrome

    […] of the cases: Hypohidrosis Occasionally present symptoms in 5-29% of the cases: Global developmental delay Hydrocephalus Short stature (Source: Kohlschutter Tonz Syndrome[dovemed.com] […] of the cases: Amelogenesis imperfecta Dementia Developmental regression EEG abnormality Seizures Yellow-brown discoloration of the teeth Frequently present symptoms in 30-79%[dovemed.com]

  • Neurogenic Arthrogryposis Multiplex Congenita

    […] of people have these symptoms Cachexia Wasting syndrome 0004326 Short stature Decreased body height Small stature [ more ] 0004322 Percent of people who have these symptoms[rarediseases.info.nih.gov] […] appearance 0000346 30%-79% of people have these symptoms EEG abnormality 0002353 Intrauterine growth retardation Prenatal growth deficiency Prenatal growth retardation [[rarediseases.info.nih.gov] Arachnodactyly Long slender fingers Spider fingers [ more ] 0001166 Joint stiffness Stiff joint Stiff joints [ more ] 0001387 Sensorineural hearing impairment 0000407 30%-79%[rarediseases.info.nih.gov]

  • Arthrogryposis Multiplex Congenita

    […] of people have these symptoms Cachexia Wasting syndrome 0004326 Short stature Decreased body height Small stature [ more ] 0004322 Percent of people who have these symptoms[rarediseases.info.nih.gov] […] appearance 0000346 30%-79% of people have these symptoms EEG abnormality 0002353 Intrauterine growth retardation Prenatal growth deficiency Prenatal growth retardation [[rarediseases.info.nih.gov] Arachnodactyly Long slender fingers Spider fingers [ more ] 0001166 Joint stiffness Stiff joint Stiff joints [ more ] 0001387 Sensorineural hearing impairment 0000407 30%-79%[rarediseases.info.nih.gov]

  • OSLAM Syndrome

    stature 60 33 frequent (33%) Frequent (79-30%) HP:0004322 6 clinodactyly of the 5th finger 60 33 occasional (7.5%) Occasional (29-5%) HP:0004209 7 radioulnar synostosis 60[malacards.org] […] of people have these symptoms Short stature Decreased body height Small stature [ more ] 0004322 5%-29% of people have these symptoms Clinodactyly of the 5th finger Permanent[rarediseases.info.nih.gov] 80%) HP:0005518 3 abnormality of neutrophils 60 33 hallmark (90%) Very frequent (99-80%) HP:0001874 4 osteosarcoma 60 33 hallmark (90%) Very frequent (99-80%) HP:0002669 5 short[malacards.org]

  • Hypocalcemia

    Short stature, round facies, brachydactyly (Figure 3), obesity, and subcutaneous calcifications are classic features of AHO (79).[web.archive.org]

  • Pseudohypoparathyroidism Type 1A

    […] body height Small stature [ more ] 0004322 30%-79% of people have these symptoms Basal ganglia calcification 0002135 Brachydactyly Short fingers or toes 0001156 Broad 1st[rarediseases.info.nih.gov] Pseudohypoparathyroidism type 1A is caused by a spelling mistake ( mutation ) in the GNAS gene and is inherited in an autosomal dominant manner. 0000311 Short stature Decreased[rarediseases.info.nih.gov]

  • Pseudohypoparathyroidism

    […] body height Small stature [ more ] 0004322 30%-79% of people have these symptoms Basal ganglia calcification 0002135 Brachydactyly Short fingers or toes 0001156 Broad 1st[rarediseases.info.nih.gov] The first familial case of inherited 2q37.3 interstitial deletion with isolated skeletal abnormalities including brachydactyly type E and short stature. Am. J. Med.[doi.org] Pseudohypoparathyroidism type 1A is caused by a spelling mistake ( mutation ) in the GNAS gene and is inherited in an autosomal dominant manner. 0000311 Short stature Decreased[rarediseases.info.nih.gov]

  • Rothmund Thomson Syndrome

    stature Decreased body height Small stature [ more ] 0004322 30%-79% of people have these symptoms Abnormal fingernail morphology Abnormal fingernails Abnormality of the[rarediseases.info.nih.gov] Although the three syndromes share some clinical features ( e.g. short stature and radial ray abnormalities) there are also syndrome-specific features [ 80 ].[doi.org] […] atrophy Skin degeneration 0004334 Erythema 0010783 Hypopigmented skin patches Patchy loss of skin color 0001053 Irregular hyperpigmentation 0007400 Poikiloderma 0001029 Short[rarediseases.info.nih.gov]

  • Brandt Syndrome

    stature Decreased body height Small stature [ more ] 0004322 30%-79% of people have these symptoms Blepharitis Inflammation of eyelids 0000498 Cheilitis Inflammation of the[rarediseases.info.nih.gov] […] brain due to loss of brain cells 0002120 Chronic diarrhea 0002028 Dry skin 0000958 Erythema 0010783 Malabsorption Intestinal malabsorption 0002024 Pustule Pimple 0200039 Short[rarediseases.info.nih.gov]

Further symptoms