Disease #00594 (ACH (achondroplasia (ACH)), OMIM:100800)

Official abbreviation ACH
Name achondroplasia (ACH)
OMIM ID 100800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene FGFR3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-10-22 16:17:58 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00406598 Pat1 PubMed: Tamhankar 2014 2-generation family, 1 affected, unaffected parents M no India - - - - - ACH see paper; ..., short at birth; normal motor and mental milestones; height was 67.5 cm (-7.1 SD), short limbs, OFC 47 cm; acromesomelia, facial abnormalities, frontal bossing, prominent eyes, hypertelorism, flat nasal bridge, anteverted nostrils, folded low set ears, tented upper lip, wide mouth, gum hypertrophy suggestive of 'fetal facies'; thoracolumbar scoliosis, small hands, small penis (stretched penile length 1 cm), retractile testes; X-ray large cranium, crowded right sided ribs, absent left ribs 3 and 4, marked thoracic scoliosis to the right, lumbar scoliosis to the left, thoracic and lumbar hemivertebrae, short radius, short ulna; upper limb mesomelia more severe than lower limb; USG normal, ECG normal ROR2 ROR2 1 1 Johan den Dunnen
00449784 - - - - - - - - - - - ACH - FGFR3 FGFR3 1 1 Dan Feng Fang
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