Rank (Similarity) |
PMID (PMCID) |
|
---|---|---|
1 (31.0%) |
7717418 |
Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis. Toriello HV, Higgins JV. Am J Med Genet. 1995;55(2):200-4. |
Syndactyly | ||
Cleft Palate Differential Diagnosis Face Homo sapiens Infant, Newborn Intellectual Disability Male Microcephaly Phenotype Syndactyly Syndrome |
Total: 14
HPO ID | Term | Frequency |
---|---|---|
HP:0000248 | Brachycephaly | Very frequent (99-80%) |
HP:0000347 | Micrognathia | Very frequent (99-80%) |
HP:0000446 | Narrow nasal bridge | Very frequent (99-80%) |
HP:0000527 | Long eyelashes | Very frequent (99-80%) |
HP:0000574 | Thick eyebrow | Very frequent (99-80%) |
HP:0001249 | Intellectual disability | Very frequent (99-80%) |
HP:0002230 | Generalized hirsutism | Very frequent (99-80%) |
HP:0003196 | Short nose | Very frequent (99-80%) |
HP:0004322 | Short stature | Very frequent (99-80%) |
HP:0006101 | Finger syndactyly | Very frequent (99-80%) |
HP:0007477 | Abnormal dermatoglyphics | Very frequent (99-80%) |
HP:0010720 | Abnormal hair pattern | Very frequent (99-80%) |
HP:0100874 | Thick hair | Very frequent (99-80%) |
HP:0003298 | Spina bifida occulta | Occasional (29-5%) |
Total: 0
HPO ID | Term | # of case reports |
---|
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|