Phenotype #0000325269
| Individual ID |
00435027 |
| Associated disease |
DD |
| Phenotype details |
Intrauterine growth retardation (HP:0001511); Small for gestational age (HP:0001518); Short stature (HP:0004322); Motor delay (HP:0001270); Speech delay (HP:0000750); Intellectual disability (HP:0001249); Intellectual disability, mild (HP:0001256); Hypotonia (HP:0001252); Talipes equinovarus (HP:0001762); Long fingers (HP:0100807); Broad toes (HP:0001837); nail dysplasia (HP:0002164);Preauricular skin tag (HP:0000384); Periorbital fullness (HP:0000629); Hypertelorism (HP:0000316);Hypertelorism (HP:0000316); Low-set ears (HP:0000369) |
| Diagnosis/Initial |
- |
| Inheritance |
Unknown |
| Diagnosis/Definite |
- |
| Age/Examination |
11y (11 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Frederike Leonie Harms |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Frederike Leonie Harms |
| Date created |
2023-04-20 07:50:04 +02:00 (CEST) |
| Date last edited |
2023-05-24 10:30:05 +02:00 (CEST) |
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