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Prevalence (%) of clinical parameters based on data from 1 references describing 7 individuals
Add new symptom/sign to this disease
| Pubmed id number as a reference | Organ system affected | ||
| Number of patients in the reference | Percent affected patients (Between 0 and 1, eg. 0.1 = 10%) | ||
| Please provide your name and contact information as a reference | |||
| Name | Institute | Phone number | Email address |
List of symptoms
| Symptom/sign | Organ system | Percent affected | Pubmed id | Added on(yyyy-mm-dd) | Edit/add reference |
| Sloping forehead | skeletal | 100 % | 18071751 | 2015-09-18 | |
| Polydactyly | skeletal | 100 % | 18071751 | 2015-09-18 | |
| Syndactyly | skeletal | 100 % | 18071751 | 2015-09-18 | |
| Nail dystrophy | integumentary | 100 % | 18071751 | 2015-09-18 | |
| Mental retardation | nervous | 100 % | 18071751 | 2015-09-18 | |
| Microcephaly | nervous | 100 % | 18071751 | 2015-09-18 |
List of references:
A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22-q11.2.
Muhammad Jawad Hassan, Muhammad Salman Chishti, Syed Muhammad Jamal, Muhammad Tariq, Wasim Ahmad,
Human genetics - Feb 2008